Zonegran for the Treatment of Weight Gain Associated With Psychotropic Medication Use: A Placebo-Controlled Trial

Obesity Clinical Trial

— Zonegran  

Official title:

Zonegran for the Treatment of Weight Gain Associated With Psychotropic Medication Use: A Placebo-Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00203450
• Other study ID #: TREAC Zonegran for Weight Loss
• Secondary ID: TREAC Zonegran f
• Status: Completed
• Phase: Phase 4
• First received: September 12, 2005
• Last updated: August 30, 2012
• Start date: May 2003
• Est. completion date: March 2006

Study information

• Verified date: August 2012
• Source: Tuscaloosa Research & Education Advancement Corporation
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The primary objective of this study is to compare the efficacy of zonisamide (Zonegran; 100mg - 400mg/day) and placebo as an adjunctive agent on lowering weight in subjects who have a body mass index (BMI) of >25 and are on a psychotropic medication with a known side effect of weight gain.

Description:

After the screening period, patients fulfilling entrance criteria will be randomized to 100mg of zonisamide or placebo in a 2:1 ratio respectively. Patients will be assessed at baseline and on Weeks 2, 4, 8, 12, and 16-post randomization for weight, side effects, and symptoms. Symptoms will be assessed by the Young Mania Rating Scale (YMRS), Brief Psychiatric Rating Scale (BPRS), Hamilton Depression Rating Scale (HAMD), Hamilton Rating Scale for Anxiety (HARS), and Self-report measures of general health and mental status at baseline, weeks 2, 4, 8, 12,and 16. At the conclusion of the study, patients will be tapered from the study medication and will return to their primary provider for continued treatment of their psychiatric condition.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: March 2006
• Est. primary completion date: March 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 19 Years to 65 Years

Eligibility

Inclusion Criteria:

• Are men or women, between the ages of 19 and 65, inclusive

• Have a diagnosis of any type of bipolar disorder or any type of psychotic disorder based on structured diagnostic interview (MINI).

• Are currently outpatients or inpatients and taking a neuroleptic or mood stabilizer medication (listed below) for the past 6 months, and on a stable dose for the past 2 months.

• Have a body mass index > 25.

• No substance use disorder in the past 2 months (except for nicotine or caffeine).

• Agree to not become pregnant during the study and agree to use an adequate method of birth control during the study such as a barrier method, hormonal contraceptive, or surgical sterilization (females only). All women of childbearing potential must have a negative pregnancy test before beginning study medication.

• Are able to swallow the capsules whole

• Are willing and able to follow Investigator instructions and study procedures, and report adverse events

• Not currently actively suicidal or homicidal.

• No use of topiramate within the last 6 months.

• No medical contraindication to the use of zonisamide.

List of medications for inclusion criterion #3:

All conventional neuroleptics. All atypical neuroleptics except aripiprazole or ziprasidone. All forms of valproate. All forms of lithium. All forms of carbamazepine.

Exclusion Criteria:

• Clinically significant renal or hepatic disease.

• History of acute intermittent porphyria, glucose-6phosphate dehydrogenase deficiency or hemolytic anemia.

• Allergy to zonisamide or sulfonamides.

• Have clinically unstable cardiovascular, hepatic, renal, gastrointestinal, pulmonary, metabolic, endocrine, or other systemic disease

• Have laboratory test results that, in the opinion of the Investigator, are clinically significant abnormalities

• Require treatment with any medication (e.g., carbonic anhydrase inhibitors) that might interact adversely with, or obscure, the action of the study drug

• Are pregnant or lactating (females only)

• Have a history of nephrolithiasis

• Refuse to give informed consent

• Have previously enrolled in this study or previously been treated with zonisamide

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Obesity
• Weight Gain

Intervention

Drug:
• Zonegran
zonisamide
• Placebo
Placebo pill

Locations

Country	Name	City	State
United States	Tuscaloosa Research & Education Advancement Corporation	Tuscaloosa	Alabama

Sponsors (2)

Lead Sponsor	Collaborator
Tuscaloosa Research & Education Advancement Corporation	Eisai Inc.

Country where clinical trial is conducted

United States, 

References & Publications (1)

Appolinario JC, Bueno JR, Coutinho W. Psychotropic drugs in the treatment of obesity: what promise? CNS Drugs. 2004;18(10):629-51. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary objective of this study is to compare the efficacy of zonisamide (Zonegran; 100mg - 400mg/day) and placebo as an adjunctive agent on lowering weight in subjects who have a body mass index (BMI) of >25 and are on a psychotropic medication with
Secondary	NThe weight loss in patients treated with Zonisamide will be significantly greater than those treated with placebo.			No