Insulin eye drops put to the test for faster corneal healing
NCT ID NCT07812129
First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
Researchers are testing whether insulin eye drops help the cornea heal faster and reduce pain after corneal collagen cross-linking, a procedure used to treat keratoconus. In this paired-eye study, each participant receives insulin drops in one eye and standard drops in the other, so each person acts as their own control. Doctors measure the size of the corneal wound and ask about pain at several visits until the eye surface heals. The trial includes 24 adults with progressive keratoconus scheduled for cross-linking in both eyes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- insulin eye drops
- What this could lead to
- If insulin eye drops speed corneal healing, they could become a simple add-on to standard care after cross-linking and possibly other corneal injuries.
- What could go wrong
- This is a small, single-center study of 24 people with keratoconus, so results may not apply to other eye conditions or patients. Insulin eye drops can irritate the eye, and any benefit may be too small to matter in practice.
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
-
Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
-
24 people
The number who actually took part.
- Started
-
Nov 2023
- Finished
-
May 2025
- 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 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: \- Patients above 18 years old diagnosed with bilateral progressive Keratoconus with central corneal thickness more than 400 microns at thinnest location. Exclusion Criteria: * Patients with signs of infectious keratitis (bacterial, fungal, protozoal or mixed poly-microbial). * Patients with a history of herpetic keratitis or having diminished corneal sensation. * Patients with severe dry eye, apical corneal scarring, hydrops, a history of corneal surgery, or ophthalmic disease other than keratoconus. * Single eyed patients. * Patients on systemic treatment involving steroids or immune-compromised patients. * Patients who cannot be monitored with frequent visits as required in the study protocol. * Pregnant and nursing females.
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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
-
Cairo University Faculty of Medicine (Kasr Al Ainy)
Cairo, Al-Manial, 11956, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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