# Perioperative Propranolol in Patients With Post Traumatic Stress Disorder (PTSD)

> **NCT01555554** · NA · TERMINATED · sponsor: **University of California, San Francisco** · enrollment: 59 (actual)

## Conditions studied

- Post-traumatic Stress Disorder

## Interventions

- **DRUG:** Propranolol Hydrochloride
- **OTHER:** Placebo

## Key facts

- **NCT ID:** NCT01555554
- **Lead sponsor:** University of California, San Francisco
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2012-05
- **Primary completion:** 2018-06
- **Final completion:** 2019-06
- **Target enrollment:** 59 (ACTUAL)
- **Why stopped:** Unable to meet enrollment goals.
- **Last updated:** 2021-07-26

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01555554

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01555554, "Perioperative Propranolol in Patients With Post Traumatic Stress Disorder (PTSD)". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT01555554. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
