CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 149 enrolled
Drug / intervention
losartan +1 moredrug
Likely dose
Not stated in 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/NCT02709018
NCT02709018N/ACompleted

Enhancing Fear Extinction Via Angiotensin Type 1 Receptor Inhibition: A Randomized Controlled Trial in Posttraumatic Stress Disorder

University of California, San Diego·interventional·Posted Mar 15, 2016·Updated Mar 12, 2021

In Brief

A clinical study evaluating losartan and Placebo for Posttraumatic Stress Disorder. Completed, enrolled 149 participants across 6 sites.

Detailed Summary

This study is being conducted to determine if losartan, an angiotensin receptor blocker (ARB), is safe and effective in the treatment of posttraumatic stress disorder (PTSD) symptoms. The study is also intended to determine if certain genetic markers are useful in predicting PTSD symptom reduction with losartan. Approximately 160 subjects with chronic PTSD ages 18-65 will participate in this study across five sites. Subjects will be assigned by chance to take either flexibly dosed losartan (up to a maximum dosage of 100 mg) or placebo (which resembles the study drug but has no active ingredients), once a day for 10 weeks. Furthermore, it is hypothesized that CC homozygotes for rs4311 SNP in the ACE gene will have a superior response to losartan on PTSD symptoms compared to T carriers.

Study Details

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedMar 15, 2016
Enrollment StartJul 16, 2016
Primary CompletionFeb 29, 2020
Study CompletionSep 29, 2020
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 10.3 years ago

Interventions

losartandrug

Angiotensin receptor blocker (ARB)

Placebodrug

Placebo