Can pressurized oxygen tame blood sugar spikes?
NCT ID NCT04261738
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This study asks whether a single session of hyperbaric oxygen therapy (HBOT) can lower blood sugar or change glucagon levels in people with type 1 or type 2 diabetes. Participants will undergo one HBOT session and one control session (sitting in a room at normal pressure), while their blood sugar is monitored continuously and through fingersticks. The trial also checks how well a continuous glucose monitor performs during HBOT. It's a small, early study focused on short-term effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Hyperbaric oxygen therapy (HBOT) - breathing pure oxygen in a pressurized chamber
- What this could lead to
- If it works, this could point toward hyperbaric oxygen as a potential aid for blood sugar management in diabetes.
- What could go wrong
- This is a very small, early study (6 people) that only looks at short-term effects of a single session, so results may not apply broadly or lead to a treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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6 people
The number who actually took part.
- Started
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Sep 2022
- Finished
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Sep 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of type 1 or type 2 diabetes * Willing to have 2 subcutaneous glucose monitors for 10 days * Willing to be NPO after midnight on the day of the study session * Willing to come to the hyperbaric facility on successive days (one control session and one hyperbaric treatment), spending approximately 3 hours in the facility on each day of testing * Willing to undergo multiple fingersticks on the days of testing * Willing to have a peripheral intravenous catheter placed for blood sampling * Willing to perform four daily fingerstick blood glucose checks throughout the study period Exclusion Criteria: * Contraindication to HBO2 as determined by the study investigator (e.g., pregnancy) * Previous treatment with HBO2 within 30 days of enrollment * Current use of CGM is not an exclusion, but participants must use study equipment during the study * Current use of an insulin pump * Known allergy to medical-grade adhesives * Extensive skin changes/disease that preclude wearing the sensor on normal skin (e.g. extensive psoriasis, recent burns or severe sunburn, extensive eczema, extensive scarring, extensive tattoos, dermatitis herpetiformis)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Legacy Emanuel Medical Center
Portland, Oregon, 97227, United States
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