CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 34 enrolled
Drug / intervention
Olanzapine +1 moredrug
Likely dose
Olanzapine 2.5 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00260962
NCT00260962Phase 2Completed

Olanzapine in the Treatment of Low Weight and Obsessional Thinking Among Those With Anorexia Nervosa: A Double Blind Placebo Controlled Study

Ottawa Hospital Research Institute·interventional·Posted Dec 2, 2005·Updated Jan 30, 2018

In Brief

A Phase 2 clinical trial evaluating Olanzapine and Day Hospital for Anorexia Nervosa. Completed, enrolled 34 participants across 1 site.

Detailed Summary

The purpose of the study is to evaluate the efficacy of an anti-psychotic medication, Olanzapine, in achieving desired weight gain in patients identified as having Anorexia Nervosa, either restricting or binge/purge subtype. The study will also evaluate the possible beneficial effects of Olanzapine in reducing the severity of the obsessive and/or anxiety symptoms associated with this disorder.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada

Timeline

Phase 2CompletedFinished
2000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 2, 2005
Enrollment StartSep 1, 2000
Primary CompletionJul 1, 2006
Study CompletionSep 1, 2006
TodayJul 2, 2026
Enrollment to primary: 5.8 yearsPosted 20.6 years ago

Interventions

Olanzapinedrug

After a 2-week baseline period, olanzapine was administered for 10 weeks (weeks 3-12 of the study). Olanzapine was prescribed according to a flexible dose regimen, starting at the minimum dose of at 2.5 mg/day and titrated slowly by increments of 2.5 mg/week to a maximum dose of of 10 mg/day.

Day Hospitalbehavioral

Day hospital program involved attendance 4 days a week from 9:00 am to 6:00 pm for 12 to 14 weeks, and supervised meals and group therapy.