Mode
Text Size
Log in / Sign up
Phase 3 N=147 Randomized Double-blind Treatment

SSRI and Buprenorphine

Opiate Dependence · Depression

Enrolled (actual)
147
Serious AEs
0.7%
Results posted
Apr 2012
Primary outcome: Primary: Percentage of Participants Who Dropped Out of Buprenorphine Treatment — 33.3; 44.0 percentage of participants — p=.19

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
escitalopram (Drug); placebo (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Butler Hospital
Primary completion
Sep 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants Who Dropped Out of Buprenorphine Treatment
33.3; 44.0 .19
SECONDARY
Depressive Symptoms
12.31; 11.35 .18

Summary

This study is designed to test whether treatment of depressive symptoms using escitalopram improves adherence to Buprenorphine and reduces symptoms of depression for individuals receiving Buprenorphine through their medical provider.

Eligibility Criteria

Inclusion Criteria

  • opiate dependence
  • Ham-D > 14

Exclusion Criteria

  • no psychiatric contraindications to using escitalopram
  • no medical contraindications to using escitalopram
  • methadone dose < 30
  • no current SSRI use
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00475878). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search