FDA recommends UHMS-accredited hyperbaric facilities for treatment of specific illnesses
In a July 26 release entitled “Hyperbaric Oxygen Therapy: Get the Facts” the U.S. Food and Drug Administration (FDA) has cleared the use of hyperbaric oxygen therapy (HBOT/HBO2) for the treatment of several conditions. The release further states: “If your health care provider recommends HBOT, the FDA advises you get the treatment at a hospital or facility that has been inspected and is accredited by the Undersea and Hyperbaric Medical Society.”
The agency advises that individuals seeking hyperbaric oxygen therapy check with their health care provider to make sure they are pursuing the most appropriate care, noting that some facilities operate outside recognized FDA guidelines. “The FDA is aware there are some hyperbaric oxygen treatment centers promoting hyperbaric oxygen chambers for uses that have not been cleared or approved by the FDA, such as treatment of cancer, Lyme disease, autism, or Alzheimer’s disease.”
FDA-cleared conditions to be treated with hyperbaric oxygen
The FDA has cleared hyperbaric oxygen therapy for treatment in these disorders:
HBO2 treatment is being studied for other conditions, including COVID-19, but has not cleared or authorized the use of any hyperbaric device to treat COVID-19 or any conditions beyond those listed above. The websites clinicaltrials.gov and the UHMS home pages at https://www.uhms.org/images/Position-Statements/HBO2_and_COVID_8-10-2020_clinicaltrials_8-12-2020.pdf have more information on hyperbaric clinical trials for COVID-19 and other conditions.
~ Taken from MedWatch - The FDA Safety Information and Adverse Event Reporting Program
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