Tamoxifen in Treatment of Acute Mania

This study has been completed.
Sponsor:
Information provided by:
Stanley Medical Research Institute
ClinicalTrials.gov Identifier:
NCT00411203
First received: December 12, 2006
Last updated: NA
Last verified: December 2006
History: No changes posted
  Purpose

Objective: Evidence indicates that the protein kinase C-PKC signaling cascade may be one of the direct targets in treatment of mania. The aim of this study is to investigate whether the PKC inhibitor-tamoxifen has anti-manic properties. Method: Bipolar subjects with manic/mixed episode were randomly assigned to receive either tamoxifen (80mg/day) or identical placebo tablets in 1:1 ratio for three weeks.


Condition Intervention Phase
Bipolar Disorder
Drug: Tamoxifen Citrate
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Official Title: Double Blind Placebo Controlled Trial of a Protein Kinase C Inhibitor: Tamoxifen Citrate in Treatment of Acute Mania

Resource links provided by NLM:


Further study details as provided by Stanley Medical Research Institute:

Primary Outcome Measures:
  • Reduction from baseline of the Young Mania Rating Scale (YMRS) score after 3 weeks of therapy.
  • Positive treatment response, defined as >= 50% decrease in YMRS from baseline to 3 weeks.

Secondary Outcome Measures:
  • Reduction from baseline of the Clinical Global Impressions-Bipolar Version of Severity of Illness (CGI) score after 3 weeks of therapy.
  • Reduction from baseline of the Positive and Negative Syndrome Scale (PANSS) score after 3 weeks of therapy.

Estimated Enrollment: 50
Study Start Date: April 2003
Estimated Study Completion Date: June 2006
Detailed Description:

Patients aged 18-65 years, diagnosed with Bipolar Disorder (BD), most recent episode manic or mixed, with or without psychotic features were admitted to the inpatient unit at the Dokuz Eylul University, Department of Psychiatry, Izmir, Turkey. Subjects were recruited from the local community, an urban area in the western part of Turkey, surrounding suburbs, and towns as well as all over the country (expert-seeking patients who reached the principle investigator-PI, via the internet and news media) between April, 2003 and June, 2006. All diagnoses were based on the Structured Clinical Interview for the DSM-IV, administered by a trained investigator (AYY). After the protocol explained to the patient and at least one first degree relative, both gave written informed consent for participation of the patient in the trial. The study was approved by the Turkish Ministry of Health, General Directorate of Drugs and Pharmaceutics, Central Review Board, and Local Ethical Committee of Drug Investigations at the Dokuz Eylul University. Subject screening included medical and psychiatric history, physical examination, and laboratory screen including LFTs, TSH, HCG, BUN, Cr, and serum toxicology. All psychotropic medication (except benzodiazepines) was discontinued at least 1 day before randomization. Subjects entering the study were randomly assigned to receive the PKC inhibitor, tamoxifen or identical placebo tablets in a 1:1 ratio and double-blind fashion for 3 weeks. Computer-generated codes were used to create randomization kits (prepared by the ARGEFAR, Izmir, Turkey, a contract research organization). The starting dose of tamoxifen was 20 mg bid. After the first treatment day, daily dose was adjusted upward by 10 mg per day up to 80 mg/d in divided doses. Similar tablet adjustments were applied for the patients in placebo group. Concomitant use of oral lorazepam (2.5mg dissolving tables) was allowed during double-blind therapy as clinically indicated. In cases where lorazepam is thought to be ineffective and the symptoms are such that an antipsychotic is required, risperidone liquid formulations (2-6 mg/day) were used under emergency circumstances. Those subjects who were given risperidone were assumed as drop out at the time of first exposure to risperidone; and new subjects for replacement of those cases have been recruited. Subjects were seen twice daily and investigators (AYY, SG) were on call 24 hours a day.

Assessment tools; Young Mania Rating Scale (YMRS), Hamilton Depression Rating Scale-17 item (HAMD-17), Montgomery-Asberg Depression Rating Scale (MADRS), Clinical Global Impressions-Bipolar Version of Severity of Illness (CGI), and Positive and Negative Syndrome Scale (PANSS) and side effect questionnaire were administered by semi-structured interviews at each week. Vital signs and weight were monitored. The PI, who is trained in the rating instruments and blind to the treatment condition (training and certification at the Massachusetts Hospital, Bipolar Program), performed all the study assessments on a weekly basis by using all the available clinical information, provided by the prospective daily interviews by the investigators, staff reports including the security team' observations, and first degree relative reports.

Power calculations were performed to determine the sample size required to achieve 80% power to detect a difference of 0.40 in the response rate, assuming a 0.15 response rate in placebo using a chi-square test at the .05 level. Assuming 30% drop out and non compliance rate, randomization kits were prepared for 70 subjects. Following eligibility considerations and drop out the final sample size used in the analysis was 50. The primary efficacy variable is defined as the reduction from baseline of the YMRS score after 3 weeks of therapy. Positive treatment response was defined as >=50% decrease in YMRS from baseline to 3 weeks.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. diagnosis of BD I, most recent episode, manic or mixed,
  2. ages 18-65,
  3. Young Mania Rating Scale (YMRS) score > 20 at screening and baseline,
  4. providing written informed consent.

Exclusion Criteria:

  1. currently pregnant, planning to become pregnant, or breast feeding,
  2. history of any coagulopathies, deep vein thrombosis, pulmonary embolus,
  3. a history of hypersensitivity to tamoxifen,
  4. drug screen positive for any drug of abuse at screening, active substance abuse in the past 2 weeks or substance dependence in the past 2 months (except nicotine and caffeine),
  5. diagnosis of schizophrenia, dementia, delirium, seizure disorder, obsessive compulsive disorder, or major cardiac, hepatic or renal disease that is unstable or that requires medical care,
  6. administration of any other investigational drug in the last 30 days,
  7. clinically significant suicidal or homicidal ideation.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00411203

Locations
Turkey
Dokuz Eylul University, Department of Psychiatry
Izmir, Turkey, 35340
Sponsors and Collaborators
Stanley Medical Research Institute
Investigators
Principal Investigator: Aysegul Yildiz-Yesiloglu, MD Dokuz Eylul University and Harvard Medical School
  More Information

No publications provided by Stanley Medical Research Institute

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00411203     History of Changes
Other Study ID Numbers: 02T-162, AY0001
Study First Received: December 12, 2006
Last Updated: December 12, 2006
Health Authority: Turkey: Ministry of Health

Keywords provided by Stanley Medical Research Institute:
Protein kinase C, tamoxifen, acute mania, clinical trial

Additional relevant MeSH terms:
Bipolar Disorder
Affective Disorders, Psychotic
Mood Disorders
Mental Disorders
Tamoxifen
Antineoplastic Agents, Hormonal
Antineoplastic Agents
Therapeutic Uses
Pharmacologic Actions
Selective Estrogen Receptor Modulators
Estrogen Receptor Modulators
Hormone Antagonists
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Bone Density Conservation Agents
Estrogen Antagonists

ClinicalTrials.gov processed this record on April 15, 2014