Delta-THC in Dementia
|ClinicalTrials.gov Identifier: NCT01608217|
Recruitment Status : Completed
First Posted : May 31, 2012
Last Update Posted : June 30, 2014
This is a phase II, randomized, placebo-controlled, double-blind, parallel-group, multicentre study to the efficacy and safety of low dose delta-9-THC in behavioural disturbances and pain in patients with mild to severe dementia, when added to an analgesic treatment with acetaminophen.
It is hypothesized that Namisol® will lead to more behavioural disturbances than placebo, when added to an analgesic treatment with acetaminophen, and as measured by a change in Neuropsychiatric Inventory (NPI) score, after a three week treatment period.
It is expected that this will be due, primarily, to psychoactive effects of Namisol® and secondary to a reduction in pain sensation (as measured with VRS and PACSLAC-D). It is expected that a reduction in NPS will positively affect quality of life and lead to better functioning in daily living.
|Condition or disease||Intervention/treatment||Phase|
|Behavioural Disturbances Pain Dementia Alzheimer's Dementia Vascular Dementia||Drug: delta-9-tetrahydrocannabinol (delta-THC) Drug: Placebo Drug: Acetaminophen||Phase 2|
There is a high prevalence of behavioural disturbances (NPS) in persons with dementia. Persistent pain complaints can be a cause of NPS. Unfortunately, there is a lack of appropriate drugs for treating both these problems. This and positive suggestions from preliminary clinical studies with THC on NPS and directly fuel the study presented here.
This will be a phase II study in which the efficacy and safety of Namisol® (a tablet with THC) on behavioural disturbances, such as agitation, aggression and motor disturbances in dementia patients will be evaluated.
Secondary study objectives are :
2. To evaluate the efficacy of Namisol® on other secondary outcome measures, such as quality of life and functioning in daily activities.
3. To evaluate safety of Namisol® as assessed with physical examination, effects on cognitive functioning and adverse event monitoring.
4. For the subgroup of subjects suffering from pain: to evaluate the efficacy of Namisol® pain intensity
It is hypothesized that Namisol® will lead to more reduction in behavioural disturbances than placebo, when added to an analgesic treatment with acetaminophen, and as measured by a change in Neuropsychiatric Inventory (NPI) score, after a three week treatment period. It is expected that this will be due, primarily, to psychoactive effects of Namisol® and secondary to a reduction in pain sensation (as measured with VRS and PACSLAC-D). It is expected that a reduction in NPS will positively affect quality of life and lead to better functioning in daily living
This is a randomized placebo-controlled double-blind parallel-group multicentre study.
Subjects who appear to fulfill the eligibility criteria are informed about the study. After signing informed consent by the subject and/or caregiver, a screening visit will take place. Subjects who are eligible for participation enter a wash-out period, for discontinuation of their own analgesic medication (if applicable). Subjects will be randomly allocated to receive one of the two interventions (Namisol® 1.5 mg + acetaminophen 1000 mg three times daily, or placebo + acetaminophen 1000 mg three times daily) for a double-blind intervention period of three weeks. After two weeks the primary outcome measure (NPI) is assessed by a telephone interview with the caregiver. Subjects visit the site twice (at baseline and after three weeks treatment) for assessments of the outcome parameters, including the NPI. For the purpose of compliance and safety, there will be a weekly phone call, performed by the researcher. After completion of this period subject's own analgesic treatment will be restarted (if applicable). After a follow up phase of two weeks, the subject is contacted by telephone for assessment of adverse events.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||50 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||Efficacy and Safety of Delta-9-tetrahydrocannabinol (∆9-THC) in Behavioural Disturbances and Pain in Dementia|
|Study Start Date :||June 2012|
|Actual Primary Completion Date :||June 2014|
|Actual Study Completion Date :||June 2014|
Active Comparator: Namisol
Namisol is a tablet containing delta-9-tetrahydrocannabinol, the main cannabinoid from Cannabis sativa L. Namisol is added to a standardized treatment with acetaminophen.
Drug: delta-9-tetrahydrocannabinol (delta-THC)
delta-THC 1.5 mg (tablet)three times daily for a period of 3 weeks.
Acetaminophen 1000 mg three times daily for a period of 3 weeks
Other Name: Paracetamol
Placebo Comparator: Placebo
The control product is placebo, consisting of a tablet with similar appearance and taste of the test product. Placebo is added to a standardized treatment with acetaminophen.
placebo (tablet) three times daily for a period of three weeks.
Acetaminophen 1000 mg three times daily for a period of three weeks
Other Name: Paracetamol
- Neuropsychiatric Inventory (NPI) [ Time Frame: Screening, baseline, T= 2 weeks (by telephone interview) and T=3 weeks ]The NPI has been accepted as the standard measure of NPS in most clinical trials, due to high validity, good inter-rater reliability, high internal consistency and its sensitivity to drug treatment effects. In clinical practice as well as clinical research the NPI is the most commonly used instrument to assess behavioral changes. The NPI evaluates 12 behavioral domains. The frequency and severity of these behaviors is scored by the informal caregiver.
- Pain Assessment Checklist for Seniors with Limited Ability to Communicate Dutch version (PACSLAC-D) [ Time Frame: baseline (T = 0) and T= 3 weeks ]The PACSLAC-D is a brief version of Pain Assessment Checklist for Seniors with Limited Ability to Communicate in Dutch to observe pain related behavior It consists of 24 items, separated in three subscales (facial and vocal expressions, resistance/defense, social-economical aspects/mood). This scale is one of the few instruments in which the items are specifically geared towards elderly with dementia.
- Caregiver Clinical Global Impression of Change (CCGIC) [ Time Frame: baseline (T=0), T= 2 wks (by telephone interview) and T=3 wks ]The CCGIC is a 7-point Likert scale that assesses global change from baseline. The scale ranges from 1 ('very much improved') to 7 ('very much worse'). It has been frequently used in several psychopharmacological trials and in early clinical trials for antidementia drugs. When the caregiver rates the subject as changed compared to baseline, this change is, by definition, clinically meaningful.
- Cohen-Mansfield Agitation Inventory (CMAI) [ Time Frame: baseline (T=0) and T= 3 weeks ]The CMAI is selected to assess agitation and aggression. It is an internationally validated instrument, specifically developed to measure behavioral disturbance in people with dementia
- Quality of Life-Alzheimer's Disease Scale (QoL-AD) [ Time Frame: baseline (T=0) and T= 3 weeks ]The QoL-AD is a 13 -item self-report scale, using four-point Likert-scales, but can also be completed in conjunction with the interviewer. It is developed for assessment of quality of life in subjects with mild to moderate severe dementia, but there is also evidence for reliability in severe dementia.
- Barthel Index [ Time Frame: baseline (T=0) and T = 3 weeks ]The Barthel Index was originally developed to assess disability in patients with neuromuscular and musculoskeletal conditions receiving rehabilitation, but is also recommended for functional assessment in elderly. Barthel Index is an easy to conduct, 10-item scale which scores several primary activities of daily living.
- Paired Associates Learning test Wechsler Memory Scale Revised(PAL WMS-R) [ Time Frame: baseline (T = 0) and T = 3 weeks ]The PAL is a WMS subtest for assessment of episodic memory function. The PAL is sensitive to midtemporal lobe dysfunction and therefore suitable for assessment of effects of THC on hippocampal functioning. This test entails the presentation of 10 pairs of common words that have to be remembered (6 semantically related and 4 unrelated pairs). After presentation of the word pairs, the researcher reads aloud the first word of each pair, which has to be completed by the subject, thereby assessing the capacity to recall.
- Safety assessments [ Time Frame: screening, baseline (T=0), T= 3 weeks. AE and compliance during telephone calls at T= 1week, T= 2 weeks and T= 5 weeks (follow up phone call) ]Safety will be assessed by physical examination, including vital signs and internal examination. On indication extended physical (internal and neurological) examination or diagnostic tests can be performed. An ECG will be performed in all subjects during every visit. The occurrence of (serious) adverse events will be monitored, from first administration of study medication onwards. Weekly telephone calls are scheduled using a THC-specific symptom checklist to assess possible adverse events
- Verbal Rating Scale (VRS) [ Time Frame: screening, baseline, T= 3 weeks, follow up (T= 5 weeks) and daily in a medication diary ]The VRS is an ordinal self-reporting scale for assessment of pain intensity. It is a 6-point scale consisting of a list of phrases that describe increasing levels of pain intensity. The subject selects that phrase best characterizing his/her pain intensity at that moment. In agreement with the Interdisciplinary Consensus Statement on Assessment of Pain in Older Persons the VRS is chosen as the self-reporting assessment method for pain intensity in this group with mild to moderate impaired cognitive function.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01608217
|Radboud university medical center, department of Geriatrics|
|Nijmegen, Gelderland, Netherlands, 6525|
|Vincent van Gogh Institute for Psychiatry, department of Elderly|
|Venlo, Limburg, Netherlands, 5912|
|Principal Investigator:||Marcel Olde Rikkert, prof. dr.||Radboud University Medical Center Nijmegen|
|Principal Investigator:||Willem Verhoeven, Prof. dr.||Vincent van Gogh voor Geestelijke Gezondheidszorg|