New cream promises smoother recovery after eyelid surgery
NCT ID NCT07234292
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether a new preservative-free eyelid cream helps people feel more comfortable after eyelid surgery. About 30 adults who are planning eyelid surgery will use the cream twice a day for 3 months. Researchers will measure how satisfied patients are with their eyelid comfort using a simple 0-to-10 scale.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
A total of 30 patients undergoing blepharoplasty or ptosis surgery
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: * Age ≥ 18 years old * Patients planning a blepharoplasty or a ptosis surgery in at least one eye. * Patient affiliated to a health social security system * Female of childbearing potential should use a medically accepted contraceptive regimen since at least 12 weeks before the beginning of the study, during all the study and at least 1 month after the study end. Exclusion Criteria: In terms of population: * Pregnant or nursing woman or planning a pregnancy during the study. * Patient who had been deprived of their freedom by administrative or legal decision * Minor patient. * Major patient who is under guardianship or who is not able to express his non opposition. * Patient suspected to be non-compliant according to the investigator's judgment. * Patient enrolled in another clinical trial or which exclusion period is not over. In terms of associated pathology * Patient with a history or active systemic condition or receiving a medication which, in the investigator's judgment, put the patient at undue risk. * Patient suffering from a severe or progressive disease. * Patient with known or suspected hypersensitivity to one of the components of the product. Related to previous or ongoing treatment * Patient undergoing a topical treatment on the test area or a systemic treatment. * Patient under a long-term corticosteroid, NSAID or HIV therapy at the investigator appreciation. * Patient under immunosuppressive therapy * Patient under bisphosphonate therapy * Patient having Type 1 diabetes * Patient having atopic or eczema skin In terms of lifestyle * Intensive exposure to sunlight or UV-rays foreseen during the study. * Patient planning to change her/his life habits during the study. * Patient with an excessive consumption of alcohol and/or tobacco defined as: * an excessive consumption of alcohol: Drinking more than * 4 units a day for adult men and more than 2 units a day for adult women, * an excessive consumption of tobacco: ≥15-20 Cigarettes Per Day (CPD).
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Pierre-Vincent Jacomet Private Practice
RECRUITINGParis, France