PTSD Trial, Recruiting NCT01627301 Sponsor: Emory University Condition: PTSD
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PTSD Trial, Recruiting

NCT01627301
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Veterans who have been diagnosed with PTSD and have blood pressure that is either normal or slightly elevated (but not high enough to be diagnosed as high blood pressure)
  • Veterans who do not have PTSD and have blood pressure that is either normal or slightly elevated (this group would participate as a comparison group)

Who may not be able to join:

  • People who have heart disease or disease affecting the blood vessels
  • People who have used illegal drugs in the past 6 months
  • People who drink more than 2 alcoholic drinks per day
  • People who are pregnant
  • People who have a condition that affects the nervous system's control of automatic body functions, such as heart rate and blood pressure (confirm with trial site)
  • People who take certain medications that affect the sympathetic nervous system, such as clonidine (a blood pressure medication)
  • People who have taken a type of antidepressant medication called MAO inhibitors within the past 14 days
  • People who have any serious ongoing illness or medical condition

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Jeanie Park, MD, Emory University and the Atlanta VA Medical Center

Phone: 404-321-6111

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
1 July 2012
Est. completion
1 December 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in Muscle Sympathetic Nerve Activity (MSNA) Burst Frequency at Rest; Change in Baroreflex Sensitivity (BRS) at Rest; Change in MSNA Burst Frequency While Under Mental Stress; Change in BRS While Under Mental Stress

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov