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NCT00611871 · ClinicalTrials.gov registry record · Phase 2

The Use of Propranolol to Block Memory Reconsolidation in PTSD

A Phase 2 study, sponsored by Wayne State University.

Terminated
Registry status
Phase 2
Development phase
12
Enrollment target

NCT00611871 is a Phase 2 study that was terminated before completion, run by Wayne State University. The registered enrollment target is 12 participants.

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The verdict

NCT00611871, a Phase 2 study, was terminated before completion, sponsored by Wayne State University.

TERMINATED
Registry status
Phase 2
Development phase
12 participants
Enrollment target

Study Summary

The purpose of this investigation is to see if propranolol will reduce the psychophysiological hyperactivation associated with memories of combat stress in Veterans with Posttraumatic Stress Disorder.

Interventions

  • DRUG Placebo
  • DRUG Propranolol

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2007-09
Est. Completion 2015-09
Phase Phase 2

Sponsor

Wayne State University

163 total trials

What the Registry Record Tells You About NCT00611871

The ClinicalTrials.gov registry entry for NCT00611871 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wayne State University, which has 163 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00611871 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00611871 about?

NCT00611871 is a clinical study titled "The Use of Propranolol to Block Memory Reconsolidation in PTSD". The purpose of this investigation is to see if propranolol will reduce the psychophysiological hyperactivation associated with memories of combat stress in Veterans with Posttraumatic Stress Disorder.

What is the current status of trial NCT00611871?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 12 participants. The study started on 2007-09. Estimated completion is 2015-09.

What interventions are being tested in trial NCT00611871?

The interventions under investigation include: Placebo (DRUG), Propranolol (DRUG).

Who is sponsoring clinical trial NCT00611871?

This trial is sponsored by Wayne State University, which has 163 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.