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NCT01306968 · ClinicalTrials.gov registry record · Phase 2

Hyperbaric Oxygen Therapy (HBO2) for Persistent Post-concussive Symptoms After Mild Traumatic Brain Injury (mTBI)

A Phase 2 study, sponsored by U.S. Army Medical Research and Development Command.

Completed
Registry status
Phase 2
Development phase
79
Enrollment target

NCT01306968: Completed Phase 2 study, sponsored by U.S. Army Medical Research and Development Command.

NCT01306968 is a Phase 2 study that has completed, run by U.S. Army Medical Research and Development Command. The registered enrollment target is 79 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (41% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01306968, a Phase 2 study, has completed, sponsored by U.S. Army Medical Research and Development Command.

COMPLETED
Registry status
Phase 2
Development phase
79 participants
Enrollment target

Study Summary

This is a Phase II randomized trial designed to describe the magnitude of change between baseline and follow-up outcomes for symptom surveys and a battery of neuropsychological tests administered at time points corresponding before and after 10 weeks over observation in four groups: * A military population with post-concussion syndrome (mTBI) receiving local standard care * A military population with post-concussion syndrome (mTBI) receiving local standard care and sham hyperbaric oxygen sessions * A military population with post-concussion syndrome (mTBI) receiving local standard care and hyperbaric oxygen at 1.5 atmospheres sessions * A otherwise similar group with PTSD but no history of TBI receiving local standard care Differences and variability of the tests will be used for determining the optimum primary endpoint(s) for future trial, as well as for refinement of sample size and power calculations for these studies. The groups undergoing hyperbaric sessions will be assigned to receive HBO2 or sham using a randomized, double blind design. Active duty military (Army, Marine, Navy, Air Force) men and non-pregnant women residing in the United States and who will remain in the military for the entire study period, aged 18-65 years who have been deployed one or more times to the US Central Command since the initiation of Operation Enduring Freedom (October 7, 2001) who either: * have been diagnosed with Post Traumatic Stress Disorder (PTSD) as a result of traumatic events that occurred during the qualifying CENTCOM deployment, but have no diagnosed or suspected lifetime brain injuries resulting in loss or alteration of consciousness; OR * have been diagnosed with at least one mild brain injury (mTBI) with persistent (\> 4 months) symptoms sustained during one or more of those deployments

Primary Outcome

The Rivermead Post-Concussion Symptom Questionnaire (RPQ)/RPQ-3 was created to measure the severity of post-concussion symptoms following traumatic brain injury. The scale compares any current symptoms to pre-injury levels to account for potential symptom exacerbation due to the TBI. The RPQ is the most commonly used clinical outcome measure for mild TBI research because it is simple and reflects psychosocial function. The RPQ is intended to measure the presence and severity of 16 of the most co

Interventions

  • DRUG hyperbaric oxygen
  • OTHER sham hyperbaric air

Trial Details

FieldValue
Enrollment Target 79 participants
Start Date 2011-02
Est. Completion 2012-08
Phase Phase 2

What the finished NCT01306968 record still lists

NCT01306968 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 79 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (41% lower).

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

NCT01306968 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01306968 about?

NCT01306968 is a clinical study titled "Hyperbaric Oxygen Therapy (HBO2) for Persistent Post-concussive Symptoms After Mild Traumatic Brain Injury (mTBI)". This is a Phase II randomized trial designed to describe the magnitude of change between baseline and follow-up outcomes for symptom surveys and a battery of neuropsychological tests administered at time points corresponding before and after 10 weeks over observation in four groups: * A military po...

What is the current status of trial NCT01306968?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 79 participants. The study started on 2011-02. Estimated completion is 2012-08.

What interventions are being tested in trial NCT01306968?

The interventions under investigation include: hyperbaric oxygen (DRUG), sham hyperbaric air (OTHER).

Who is sponsoring clinical trial NCT01306968?

This trial is sponsored by U.S. Army Medical Research and Development Command, which has 77 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01306968's enrollment target sits among peer trials

79 884th of 2000 higher than 1,117 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01306968, the US trial registry maintained by the National Library of Medicine. NCT01306968 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.