drugset / Trial / NCT00371176
A Placebo-Controlled Trial of D-Cycloserine and Exposure Therapy for Combat-PTSD
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The primary aim of this project is to examine whether administration of D-Cycloserine (DCS), a partial N-methyl-D-aspartate (NMDA) receptor agonist that has been shown to facilitate fear extinction, enhances the therapeutic benefit of exposure-based cognitive behavioral therapy (CBT) in OEF/OIF veterans with PTSD.
Timeline
- Start
- 2006-10
- Primary completion
- 2011-09
- Completion
- 2012-07
Outcome
Missed primary endpoint
paper results indicated that veterans in the exposure therapy plus DCS condition experienced significantly less symptom reduction than those in the exposure therapy plus placebo condition over the course of the treatment. PMID 22694905 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cycloserine | Small molecule | 50 mg | — |