What Researchers Did
Researchers reported safety monitoring data from two randomised double-blind HBOT trials involving 143 military personnel with post-concussive symptoms, receiving either HBOT at 1.5 ATA or sham at 1.2 ATA across 4,245 total chamber sessions.
What They Found
Adverse events were rare: 1.1% of sessions in HOPPS and 2.2% in BIMA. Minor barotrauma (ear pressure effects) was the most common complaint. No serious chamber-related adverse events occurred. The sham control successfully preserved blinding throughout both trials.
Canadian Relevance
No direct Canadian connection identified.
Study Limitations
The study population was entirely US military personnel; adverse event rates may differ in civilian populations with different health profiles or treatment protocols.