Simple eye bandage may speed healing after eyelid lift

NCT ID NCT07701265

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 14, 2026 · Last updated Jul 15, 2026 · Updated 1 time

Summary

This study tests whether wearing a compression dressing for 24 hours after upper eyelid blepharoplasty (eyelid lift) reduces swelling, bruising, and pain. Each participant has both eyelids operated on; one eye gets the dressing, the other does not. Masked observers assess recovery at 1, 7, 30, and 90 days after surgery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
a compression dressing (sterile gauze pads secured with elastic tape) applied for 24 hours after surgery
What this could lead to
If effective, this simple, low-cost dressing could become a standard part of recovery after eyelid surgery, reducing swelling and bruising for patients.
What could go wrong
This is a small, single-center trial with 56 participants, so results may not apply to all patients. The dressing might not provide significant benefit over standard care.

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

56 people

The number who actually took part.

Started

Jun 2025

Finished

Nov 2025

Lead sponsor

A government agency

The lead sponsor is a government body.

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adult patients (≥18 years) with bilateral upper eyelid dermatochalasis scheduled for upper eyelid blepharoplasty * Willingness and ability to provide written informed consent * Ability to comply with the postoperative follow-up schedule (postoperative days 1, 7, 30, and 90) Exclusion Criteria: * History of prior upper eyelid surgery * Unilateral dermatochalasis * Previous eyelid trauma * Congenital eyelid anomalies * Blepharochalasis syndrome * Coagulopathy * Combined indication for ptosis repair and blepharoplasty * Severe bilateral visual impairment precluding safe application of compression dressing

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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

  • Beyoglu Eye Training and Research Hospital

    Istanbul, Istanbul, 34421, Turkey (Türkiye)

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Other studies related to the condition(s) this trial covers.