The German Project of Heroin Assisted Treatment of Opiate Dependent Patients
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00268814|
Recruitment Status : Completed
First Posted : December 22, 2005
Last Update Posted : September 9, 2015
|First Submitted Date ICMJE||December 21, 2005|
|First Posted Date ICMJE||December 22, 2005|
|Last Update Posted Date||September 9, 2015|
|Study Start Date ICMJE||March 2002|
|Actual Primary Completion Date||December 2003 (Final data collection date for primary outcome measure)|
|Current Primary Outcome Measures ICMJE
|Original Primary Outcome Measures ICMJE
|Current Secondary Outcome Measures ICMJE
|Original Secondary Outcome Measures ICMJE
|Current Other Pre-specified Outcome Measures||Not Provided|
|Original Other Pre-specified Outcome Measures||Not Provided|
|Brief Title ICMJE||The German Project of Heroin Assisted Treatment of Opiate Dependent Patients|
|Official Title ICMJE||Phase III Study of Maintenance Treatment for Opiate Dependence With Heroin (Diamorphine) Compared to Methadone|
The study will test the hypotheses that heroin assisted treatment, compared to methadone maintenance treatment, is more effective with regard to
The medication is injectable pure heroin (diacetylmorphine) 3x/d, or d l methadone 1x/d
The study design is multicentre, open, randomised, 4 x 2 stratified. The study duration is 24 months (individual period of investigation), 1. study phase: 12 moths (protocol part B) and 2. study phase: 12 moths (part C). Patients recruited have an opiate dependency according to ICD-10, who are not being treated currently or who are in a methadone maintenance programme with an unsatisfactory course of treatment.
Detailed description of study phase 1 (randomized, controlled part of study) only.
Part B - Study phase 1 B1.1 Clinical hypothesis Compared to maintenance with oral methadone, heroin treatment leads to
B1.2 Primary outcome criteria
B2.2 Recruitment of patients The period of registration is not part of the individual study period. A screening is carried out at registration concerning certain inclusion criteria. The patients are given the opportunity of a thorough information concerning the conditions and course of the study.
First of all, patients are asked to sign their consent to participate in the study. This is followed by the indication assessment (T-1) by the study physician and the external interview (EuropASI). Certain (particularly medical) characteristics are again examined at the beginning of treatment (T0).
The regionally responsible study physician will decide on the inclusion in the study. His decision needs the confirmation of a regional committee of experts.
B2.3 Randomisation The allocation to treatment places of the experimental or control group is carried out according to a randomisation code. Randomisation is done separately for both groups (MS and NE) based on permuted blocks of fixed size.
After the evaluation of the indication assessment and the first interview (at T-1), patients who have been recruited and who fulfil the inclusion criteria are then asked to give a second consent of participation in the study, and the results of randomisation will be communicated to them.
B2.4 Course of the study, examinations and times of the investigations The first phase of the clinical trial covers a period of 12 months. All questioning is done in a personal interview ("face to face") with the assurance that all information will be confidential.
All patients who take part in the interviews receive an expense allowance of Euro 15.- for each survey.
A hair sample is already taken at the indication examination (T-1). This allows taking a hair sample fit for analysis at the beginning of treatment (T0) from those patients whose hair was too short at T-1. The CIDI will be carried out after one month of treatment in order to minimise initial influences requiring treatment.
In order to determine the use of illicit heroin, which is a main target criterion, five urine controls will be thoroughly examined by GC/MS both in the 6th and the 12th month of treatment.
B3. PATIENTS The adequate treatment of the questions posed by this study requires a number of at least 140 patients in each test group (4 experimental and 4 control groups). Therefore, the sample size for the entire study will be N=1,120.
B3.1 Inclusion criteria
Patients who fulfil following criteria can be included in the study:
Persons with at least one of the following criteria cannot be included in the study:
B3.3 Dropping out of treatment
Participation in the study is voluntary i.e. the patient can withdraw his consent to be treated (and to further participation in the study) at any time. Patients having at least one of the following characteristics are removed from treatment:
B4.3 Dose regimen Heroin (in combination with methadone) An additional medication of d-1 methadone at night will be offered from the start, i.e. on the second day of treatment at the earliest. The administration of heroin will occur up to 3 times a day during the opening hours of the setting, in the morning, at noon and in the evening. In accordance with the Swiss and Dutch studies, the maximum daily dose of i.v. heroin will be 1,000 mg, the single dose 400 mg. If methadone is claimed at night, it can be taken on the premises during the evening opening hours or taken out as a drinkable, not injectable single dose. The daily maximum dose of additionally prescribed d,l methadone should not exceed 60 mg. Methadone consumption will be controlled by regular urine analyses.
Heroin will be handed out as injectable single doses (in filled syringes) and administered by the patient himself under observation. Patients should stay in the centre for at least 30 minutes after the injection, in order to control for possible unwanted effects.
The different dose regimens (dose regulation at the beginning of treatment or after interruptions starting from different points, fading out in case of (un-)planned treatment conclusions) are based on methadone daily equivalence doses (MTQ). According to the basic rule of the different dose regimens, an individual dose of i.v. heroin for one day, alone or in combination with oral methadone, must not exceed the MTQ of the previous day by more than 50%.
Methadone Oral methadone will be administered once a day. It is taken on the premises under observation as drinkable, not injectable single dose. There is no fixed maximum daily dose; according to experience, dosages between 40 and 160 mg/d of methadone (in individual cases up to 250 mg/d) must be expected. A 1% methadone HCL solution is recommended.
Dose regimen at the conclusion of treatment The conclusion of treatment is done by a step-by-step discontinuation of i.v. heroin or change to oral methadone. The discontinuation of medication (i.v. heroin alone or in combination with methadone) will be done slowly. Preferably, the reduction should not be more than 10%-20% of the MTQ of the previous day. In most cases discontinuation can be completed within 2 weeks. Possible withdrawal symptoms can be treated by concomitant medication.
B5. VARIABLES B5.1 General patient characteristics General and specific sample characteristics such as gender, age, length of opiate dependency, number of previous treatments, current social situation are documented.
B5.2 Medical examination and prescription data, laboratory parameters The daily amounts of heroin or methadone handed out are registered and all further prescriptions are documented. Medical examinations are documented in the CRF.
B5.3 Pharmacokinetics Since pharmacokinetics, the analgetic effects, the tolerance effects and the addiction potential of heroin are well known and new findings are not to be expected within the framework of this study, the study focuses mainly on questions concerning the effects and safety of medication.
B5.4 Efficacy Primary outcome variables Efficacy is investigated with regard to two primary outcome measures - improvement of the state of health (A) and reduction of illicit drug consumption (B). These criteria will be evaluated independently by the statistical comparative analysis; the success of one treatment in comparison to the other treatment is only proven, if both analyses have significant results pointing in the same direction.
State of health (A)
A1. Physical state of health:
Number of symptoms according to the health scale of the Opiate Treatment Index OTI at T 1 and T12.
VA1n = OTI-Health Scale (0 ≤ VA1n ≤ 50).
A2. Mental state of health:
Global Severity Index GSI of the SCL-90-R at T 1 and T12. VA2n = GSI value (0 ≤ VA2n ≤ 4).
The treatment response concerning the improvement of the state of health is given, if one of the two criteria (VA1 or VA2) shows an improvement and the other criteria shows no aggravation. Improvement and aggravation are defined as follows:
Illicit drug consumption (B)
B1. Use of illicit heroin:
Number of illicit heroin-positive urine analyses during the 12 months of treatment, i.e. among the last 5 urine samples before T12.
VB1n = number of positive urine samples (0 ≤ VB1 ≤ 5). If the patient has dropped out of treatment, and results at T12 are missing and the LOCF procedure is not possible because of missing urine samples in the 6th month of treatment, but if at least one follow-up has occurred within the ITT method, the patient's self-reported data on use of illicit heroin (physician-CRF) will be used. If these are also missing, self-reported data from the external interview can be used. This will be based on the number of days with illicit heroin consumption during the last 30 days (VB1') before the corresponding time of investigation.
VB1'n = number of illicit heroin consumption days (0 ≤ VB1' ≤ 30).
B2. Cocaine use:
Cocaine concentration of hair based on hair analyses (HAs) at T-1 and T12 within following proof limits:
VB2 n = cocaine concentration (VB2 n ≥ 1 μg/g). If the patient has dropped out of treatment, if results at T12 are missing and the LOCF procedure is not possible because of missing HA at T6, but if at least one follow-up has occurred within the ITT method, the patient's self-reported data on cocaine consumption (physician-CRF) will be used. If these are also missing, self-reported data from the external interview can be used. This will be based on the number of days with cocaine use during the last 30 days (VB2') before the corresponding time of investigation.
VB2'n = number of cocaine consumption days (0 ≤ VB2' ≤ 30). HA does not represent the frequency but the integral intensity within the (past) period of observation assuming an average hair growth of 10 mm per month. The lower limit of proof is assumed to be 1μg/g. An increase of cocaine consumption can be accurately proven, if the value at T12 has increased by 30% in comparison to T-1. (If the hair is too short - less than 1.5 cm - to take a sample at T-1, it will be done at T0.)
Decrease and non-increase of consumption are defined as follows:
It has to be assumed that a certain number of patients will prematurely (before initiation of treatment or within the first 3 months) drop-out of treatment (in the case of methadone about 20% up to 40%, in the case of heroin 10%-20%), but that they can be reached again for the examinations and investigations. These patients can be summoned for examination at the fixed times, but 5 urine samples during the last month will not be available from them. These patients without valid data are rated as non-responders in the heroin group and as "worst case" responders in the methadone group. Thus, because a rather high percentage of dropouts in the control group have to be expected, it would be hardly possible to prove the su¬periority of the experimental treatment. In that case, the (negative) result of the study would be caused by problems attributable to the implementation and measuring circumstances of the target criteria so that the evaluation of changes cannot be carried out adequately. Under the specified evaluation strategy, the procedure of measuring the consumption primary outcome measures exclusively by objective methods cannot be maintained.
If 5 urine samples are required within a defined period and 2 at most may be positive, a deviation of this pattern (e.g. urine samples are missing or cannot be used, the patient does not turn up any more) prevents that the primary outcome measures can be reliably investigated and documented. If this happens at T12, a compensation with data at T6 is possible (LOCF). It must be assumed, however, that dropouts occur most often during the first weeks, days or even im¬mediately before the beginning of treatment so that a great number of patients never reaches point T6 for the necessary objective measuring; therefore, it is not realistic to summon dropouts for urine samples 5 times with weekly intervals during the 6th and the 12th month.
An increase of cocaine use is proven by hair analyses (HA). It must be expected also in this case that, for various reasons, a certain number of patients (though much less) will not provide a hair sample at T6 or T12.
Therefore, missing or not useable data concerning the primary outcome measures of illicit heroin use (VB1) and cocaine use (VB2) respectively will be compensated by the patient's report on his consumption during the last 30 days. This procedure is as objective as possible; results are only compensated by subjective data in exceptional cases (dropouts, incorrect or missing data).
The general treatment response is shown by an improvement of the state of health (physical or mental symptoms) and by a decrease of illicit heroin consumption as well as by the non-increase of cocaine consumption between the beginning of treatment and the conclusion of phase 1 of the study.
B5.5 Safety Serious adverse events (SUE), adverse events (UE) and side effects (UAW) must be recorded consistently throughout the study. Side effects will be investigated quantitatively. At each investigation, following effects and side effects related to intoxication will be examined routinely.
The blood controls carried out within the study will be checked for laboratory test abnormalities. Such changes will be documented in the CRF and added to the adverse events (UE) and, if applicable, to the unwanted side effects (UAW).
B6. STATISTICAL ANALYSES B6.1 Safety analysis Under inclusion of all persons who have been randomised, an analysis of emergencies, adverse events (UE) and serious adverse events (SUE) will be carried out. With regard to such events (prevalence, severity classification) potential group differences will be checked for statistical significance.
B6.2 Efficacy analysis The primary outcome analysis will be carried out according to the "intention to treat" principle (ITT), which includes all randomised patients, i.e. all patients who were assigned to one of the treatment groups after twice repeated written consent. With regard to the 4 x 2-branched study design, a 4-factorial logistic regression model will be used. In case of missing information, the "last observation carried forward" method (LOCF) will be applied.
Primary outcome analysis For the experimental and the control groups, this proof of superiority of heroin will be furnished by a 4-factorial logistic regression model; two separated analyses will be calculated for the criterion "improvement of the state of health" (A) and for the criterion "reduction of illicit drug consumption" (B).
An overall success of the study (proof of the superiority of heroin treatment compared to methadone treatment) is assumed if, both for the main target criterion (A) "improvement of the state of health" and the main target criterion (B) "reduction of illicit drug consumption", a superiority of heroin treatment in comparison to methadone treatment can be proven in the respective logistic regression model with an α-error of 5%.
Primary outcome criterion (A) - Improvement of the state of health:
H0A: OR ≤ 1 (Response rate in heroin treatment ≤ Response rate in methadone treatment), H1A: OR > 1 (Response rate in heroin treatment > Response rate in methadone treatment).
The hypothesis is tested one-tailed with a 2.5% alpha error level.
Primary outcome criterion (B) - reduction of illicit drug consumption:
H0B: OR ≥ 1 (Rate of illegal drug use in heroin treatment ≥ in methadone treatment), H1B: OR < 1 (Rate of illegal drug use in heroin treatment < in methadone treatment).
This hypothesis is also tested one-tailed with a 2.5% alpha error level.
Proof of the overall effect of heroin treatment:
The experimental treatment (controlled heroin treatment) will be rated to be successful, if the logistic regression has following results:
Secondary outcome analyses The secondary evaluations are carried out according to the scale levels of the variables or of the indices formed (maintenance rate, drug consumption, scene contacts, delinquency, housing situation, social contacts, quality of life, mortality rate), i. e. by bivariate or multivariate analyses.
B6.3 Sample size determination
The calculation of the sample size is based on following efficacy expectation:
• Primary outcome criterion (A) - improvement of the state of health: Efficacy expectation in control groups: ≤ 30% of responders, Efficacy expectation in experimental groups: > 50% of responders.
• Primary outcome criterion (B) - reduction of illicit drug consumption: Efficacy expectation in control groups: ≤ 30% of responders, Efficacy expectation in experimental groups: > 50% of responders. Within the framework of the 4 x 2-branched study design, each primary outcome criterion will be analysed by a 4-factorial logistic regression analysis. With the (conservative) assump¬tion that both target criteria are stochastically independent, a power of 90% for each main out¬come criterion guarantees that a (multiple) total power of 80% is maintained [(1-β)2 ≈ 0.80 for β = 0.10]. Since the total success of the study is only assumed if treatment effects are evident for both primary outcome measures, a correction of type-1-error is not necessary.
A certain number of patients will (prematurely) drop-out of treatment and not be included in the evaluation by LOCF, because they cannot be reached any more for examinations and interviews. These are patients who dropped out prior to T6 or have not started treatment or refused their consent to the investigation of the two primary outcome variables. According to the conservative evaluation strategy, these patients must be treated as "worst cases". Therefore, the size of the assumed effect decreases in relation to the percentage of these "not reached" patients in the heroin and methadone group. Realistic estimations of these percentages are 10% drop-outs in the methadone group and 5% in the heroin group. According to these expected percentages, the estimated effect size on which the calculation of the sample size is based, is reduced from 0.3 vs. 0.5 to 0.370 vs. 0.475.
Based on this assumption, a multiple total power of 80% requires a number of cases of at least N=482 test persons for each sample group (based on Chi2-test for odds ratio, sample size approximation according to Nam 1992). Related to the individual strata, this means at least four heroin and four methadone strata with at least 121 patients each are necessary to prove the expected effect with a statistical power of 80%. For practical reasons (adequate distribution to the study cen¬tres, increased measuring precision), this number is rounded up to N=140 resulting in eight strata with a total number of N=1,120 patients.
Under the described conditions, this sample size guarantees that in both tests a significant difference between methadone and heroin treatment can be proven with a statistical total power of at least 80%.
B6.4 Missing data If data of the 12-months examination are missing and concern the primary outcome criteria and cannot be replaced by the LOCF method, a non-fulfillment of the criterion must be assumed, which will be interpreted as "worst case" in the individual case.
B6.5 Drop-outs Patients dropping out of treatment will continue to be included in the investigations and evaluations (ITT-analysis). According to the LOCF method, the latest information of each patient will be used for the analysis if a patient cannot be interviewed at the conclusion of the study. As far as the primary outcome criterion of illicit heroin consumption is concerned, the 12-month information can only be completed by the investigation at T6, because only the five urine samples in the 6th month of treatment can be tested for illicit heroin by GC/MS. Similarly, a missing hair analysis for cocaine consumption at T12 can only be completed by a hair sample precautiously taken at T6. If no objective measure results of the primary outcome measures illicit heroin and cocaine consumption are available, the patient's self-report will be included in the analysis.
Patients who did not participate in any further investigation after the inclusion in the study are rated as "worst case", i.e. not reached patients of the methadone group are rated as success (responders) and not reached patients of the heroin group as failures (non-responders). Patients who died in the first phase of the study are rated (in the experimental and the control group) as non-responders. Patients, who withdraw their consent after randomisation and do not initiate the study treatment, are excluded from the ITT-analysis.
|Study Type ICMJE||Interventional|
|Study Phase ICMJE||Phase 3|
|Study Design ICMJE||Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
|Condition ICMJE||Opioid Dependence|
|Study Arms ICMJE||
|Publications *||Not Provided|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Recruitment Status ICMJE||Completed|
|Actual Enrollment ICMJE
|Original Enrollment ICMJE
|Actual Study Completion Date ICMJE||December 2007|
|Actual Primary Completion Date||December 2003 (Final data collection date for primary outcome measure)|
|Eligibility Criteria ICMJE||
|Ages ICMJE||23 Years and older (Adult, Older Adult)|
|Accepts Healthy Volunteers ICMJE||No|
|Contacts ICMJE||Contact information is only displayed when the study is recruiting subjects|
|Listed Location Countries ICMJE||Germany|
|Removed Location Countries|
|NCT Number ICMJE||NCT00268814|
|Other Study ID Numbers ICMJE||ZIS-HV9-0701|
|Has Data Monitoring Committee||Yes|
|U.S. FDA-regulated Product||Not Provided|
|IPD Sharing Statement ICMJE||Not Provided|
|Current Responsible Party||PD Dr. Uwe Verthein, Universitätsklinikum Hamburg-Eppendorf|
|Original Responsible Party||Not Provided|
|Current Study Sponsor ICMJE||Universitätsklinikum Hamburg-Eppendorf|
|Original Study Sponsor ICMJE||University of Hamburg-Eppendorf|
|PRS Account||Universitätsklinikum Hamburg-Eppendorf|
|Verification Date||September 2015|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP