drugset / Trial / NCT00305500

Tolerability and Efficacy of High Dose Escitalopram for the Treatment of Obsessive-Compulsive Disorder (OCD)

NCT00305500

Phase 3 Completed 100 enrolled Abarbanel Mental Health Center
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Objectives: To evaluate tolerability and efficacy of escitalopram treatment in high dose than 20-50 mg/d in out-patients with OCD Type of the study: Open label, prospective study. Number of patients: 100 patients with OCD Duration of the study: 18-weeks of active treatment, 8-visits: Dose titration: One week of 10mg Four weeks of 20mg After 4 weeks of 20mg treatment- if partial/no response, according to YBOCS score and clinical judgment, dose increase of up to 50mg depending on response, adverse events, patient preference and judgment of the clinician 12 weeks follow up on high dose. Total of 18 weeks of follow-up.

Timeline

Start
2006-03
Primary completion
Completion
2006-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Escitalopram Small molecule 50 mg