Insulin gel mends ear drums faster in small trial
NCT ID NCT07535827
First seen Jun 25, 2026 · Last updated Sep 04, 2026 · Updated 6 times
Summary
This early-phase trial tested a special insulin gel applied directly to the ear drum after surgery to repair a long-standing hole. Fifty adults with dry ear drum perforations received either the insulin gel or a plain foam control. The insulin group showed significantly better healing at follow-ups up to two months. While promising, the study is small and early, so more research is needed.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- insulin gel (applied directly to the ear drum)
- What this could lead to
- If confirmed in larger trials, this insulin gel could become a simple, low-cost way to help ear drum perforations heal faster after surgery.
- What could go wrong
- This was a very small, early-phase trial (50 people). The results need to be repeated in larger, longer studies before we know if it really works safely.
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
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
-
50 people
The number who actually took part.
- Started
-
Mar 2026
- Finished
-
May 2026
- Lead sponsor
-
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
-
18 to 50 years
- Sex
-
Anyone
- Healthy volunteers
-
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: * aged 18 years or older, * with a confirmed diagnosis of tubotympanic CSOM without discharge for at least three months, * an intact ossicular chain, normal middle ear mucosa on otoscopic or endoscopic examination, * conductive hearing loss indicated by an air-bone gap less than 30 dB Exclusion Criteria: * unfit for general anesthesia, * had cervical spine disorders limiting operative positioning, * active otorrhea, granulation tissue, or mucosal inflammation
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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
-
Minia university hospital
Minya, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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