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NCT02226367 · ClinicalTrials.gov registry record · NA

Prazosin Augmentation of Outpatient Treatment of Alcohol Use Disorders in Active Duty Soldiers With and Without PTSD

A NA study, sponsored by Seattle Institute for Biomedical and Clinical Research.

Completed
Registry status
NA
Development phase
158
Enrollment target

NCT02226367 is a NA study that has completed, run by Seattle Institute for Biomedical and Clinical Research. The registered enrollment target is 158 participants.

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The verdict

NCT02226367, a NA study, has completed, sponsored by Seattle Institute for Biomedical and Clinical Research.

COMPLETED
Registry status
NA
Development phase
158 participants
Enrollment target

Study Summary

The purpose of the study is to evaluate if the drug prazosin: * will decrease alcohol use in active duty members of the military who served in Iraq and/or Afghanistan and * determine if presence or absence of posttraumatic stress disorder affects treatment.

Interventions

  • DRUG placebo
  • DRUG prazosin hydrochloride

Trial Details

FieldValue
Enrollment Target 158 participants
Start Date 2015-01
Est. Completion 2018-10-20
Phase NA

What the Registry Record Tells You About NCT02226367

The ClinicalTrials.gov registry entry for NCT02226367 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 158 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Seattle Institute for Biomedical and Clinical Research, which has 43 total studies on file at ClinicalTrials.gov.

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

NCT02226367 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02226367 about?

NCT02226367 is a clinical study titled "Prazosin Augmentation of Outpatient Treatment of Alcohol Use Disorders in Active Duty Soldiers With and Without PTSD". The purpose of the study is to evaluate if the drug prazosin: * will decrease alcohol use in active duty members of the military who served in Iraq and/or Afghanistan and * determine if presence or absence of posttraumatic stress disorder affects treatment.

What is the current status of trial NCT02226367?

This trial is currently completed. It is a NA study. The enrollment target is 158 participants. The study started on 2015-01. Estimated completion is 2018-10-20.

What interventions are being tested in trial NCT02226367?

The interventions under investigation include: placebo (DRUG), prazosin hydrochloride (DRUG).

Who is sponsoring clinical trial NCT02226367?

This trial is sponsored by Seattle Institute for Biomedical and Clinical Research, which has 43 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.