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Study ID: NCT00606411

Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Determine the Efficacy and Safety of Topiramate in the Treatment of Sleep-Related Eating Disorder

Status:
Recruiting
Phase:
0

Trial Contact Information

Principal Contact:
Kate Miley
Principal Phone:
617-783-1496
Principal Email:
jwwinkelman@partners.org

Sponsor(s): Brigham and Women's Hospital

Condition(s):
Eating Disorders
Sleep Disorders
Eating Disorder

Purpose: The purpose of the study is to learn about the safety and effectiveness of oral (taken by mouth) topiramate in treating Sleep-Related Eating Disorder (SRED).

Eligibility:
Minimum Age:
18 Years
Maximum Age:
65 Years
Accepts Healthy Volunteers:
No

Inclusion Criteria:

- Adults 18-65

- Diagnosis of SRED

- Must be able to swallow capsules and follow instructions

Exclusion Criteria:

- Women who are pregnant or lactating

- Other sleep disorders

- Kidney or Liver disease

- Night shift workers

- History of non-response or adverse reactions to topiramate

Other Location(s): Brighton, Massachusetts United States

Terms: This is an abstract courtesy of ClinicalTrials.gov, a service of the US National Institute of Health Developed by the National Library of Medicine. ClinicalTrials.gov provides regularly updates information about federally and privately supported clinical research in human volunteers.

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