Hyperbaric Oxygen Effects on Persistent Post-concussive Symptoms
Completed · Phase 2 · Has a placebo group
Conditions studied: Persistent Post-concussive Syndrome, Concussion Post Syndrome
In brief
Persistent post-concussive symptoms (PPCS) are a source of significant burden among a subset of patients with concussion with prevalence rates previously reported between 11 - 82% based on timing of assessment, diagnostic criteria, or population under study. Examples of persistent post-concussion symptoms include balance problems, headaches, fatigue, poor concentration, forgetfulness, anxiety, irritability, and sleep disturbance. Few proposed therapies have proved successful in the management of persistent post-concussion symptoms following mild traumatic brain injury. The investigators will explore hyperbaric oxygen administered in a randomized sham-controlled clinical trial as an effective and tolerable treatment in improving neuropsychological status among adult patients with persistent post-concussive symptoms. The overall hypothesis to be evaluated is that hyperbaric oxygen improves neuropsychological status and a serum concussion biomarker associated with PPCS.
Key facts
- Study ID
- NCT05173818
- Run by
- Essentia Health
- People needed
- 20
- Starts
- 2022-06-28
- Expected to finish
- 2025-08-01
- Last updated by the study team
- 2025-12-24
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Volunteers must have a history of mild traumatic brain injury, specifically, persistent post-concussive symptoms after examination by a neuropsychologist or neurologist.
- Volunteers time from concussive incident (Mild traumatic brain injury) must be between 3 months - 5 years following head trauma incident
- TBI was caused by non-penetrating trauma
- Volunteers must have current complaints of TBI symptoms such as headache, dizziness, or cognitive or affective problems
- Volunteers must be 18-year-old or more
- Willing and able to provide informed consent
- Able to speak and read English, as primary language
- Agrees to provide blood samples for clinical lab tests
- Willing and committed to comply with research protocol and complete all outcome measures
- Able to equalize middle ear pressures or willing to undergo needle myringotomies if needed
- Willingness and committed to comply with study protocol outlined reproductive plan based on baseline reproductive status
You may not qualify if…
- Prior treatment with hyperbaric oxygen treatment
- Hyperbaric chamber inside attendant, professional, SCUBA diver (technical, commercial, operational/military or recreational)
- The investigators will exclude pregnant women from this study because potential fetal adverse reactions triggered by high oxygen partial pressures such as retrolenticular fibroplasia though careful review of human data are generally reassuring such as the use of hyperbaric oxygen to treat acute carbon monoxide poison in the pregnant patient.13
- Prisoners
- Minors
- Unable to protect airway or requires frequent suctioning
- Known or suspected peri-lymphatic fistula
- Presence of tracheostomy (due to limitations in auto-inflating the middle ear)
- Unable to participate fully in outcome assessments
- Unable to cooperate with hyperbaric oxygen treatments
- Unable to speak and read English, as primary language
- Not cooperating with instructions during hyperbaric oxygen treatments such as bringing contraband items into the chamber (such as fire lighter)
- Not competent to sign their own consent. Such potential participants will not have the capacity to participate in a full range of neurocognitive testing
- Pre-existing diagnosis of a psychotic disorder(s): schizophrenia, bipolar, dissociative disorder
- History of moderate or severe traumatic brain injury
- History of brain injury not of traumatic etiology such as stroke or drug-induced coma
- Verifiable diagnosis of learning disability. Other pre-existing cognitive issues may make it difficult for potential participants to fill out certain outcome assessments such as neurobehavioral symptomatic inventory. This could lead to measurement bias or confound the result.
- Claustrophobia and unwilling to enter hyperbaric chamber
- Untreated pneumothorax
- Presence of implanted device with un-verifiable test to pressure by manufacturer
- Concurrent enrollment in an alternate interventional trial for post concussive symptoms
Where it is running
- Essentia Health — Fargo, North Dakota, United States
Full record on ClinicalTrials.gov
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