Tiny corneal pockets tested as Suture-Free seal for cataract incisions

NCT ID NCT07821203

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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 Results may not be published yet.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

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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 15, 2026 · Last updated Sep 16, 2026 · Updated 1 time

Summary

Researchers at the Philippine Eye Research Institute studied a surgical technique called a sub-incisional pocket (SIP) for sealing the small corneal incisions made during cataract surgery. The study reviewed records from 35 adults who had routine phacoemulsification with a clear corneal incision. The team graded how well the wounds sealed on the first day after surgery and tracked changes in astigmatism over time. The goal is to see whether this pocket technique offers a safe and effective way to close corneal wounds without stitches.

What this could mean

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

Active substance
Sub-incisional pocket (SIP), a surgical wound-sealing technique using two non-penetrating corneal incisions placed before the main cataract incision
What this could lead to
If the technique seals incisions reliably, it could offer cataract surgeons a simple way to close corneal wounds without sutures and possibly reduce post-surgery astigmatism.
What could go wrong
This is a small retrospective study of 35 eyes, so it cannot prove the technique works better than standard care. Results may not apply to other surgeons, and the study cannot rule out complications that appear later.

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.

Participants

35 people

The number who actually took part.

Started

Jan 2025

Finished

Feb 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.

Who is studied

Patients that have undergone phacoemulsification with the sub-incisional pocket (SIP) from the Peregrine Eye and Laser Institute within the set study period of January 1, 2025 to February 28, 2026.

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Anyone

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 (≥18 years) participants * Patients undergoing primary phacoemulsification with clear corneal incision and in-the-bag intraocular acrylic lens * Uncomplicated cataract surgeries utilizing a 2.2 mm temporal clear corneal incision with sub-incisional stromal pocket. Exclusion Criteria: * Medical records from patients with intraoperative complications requiring incisions or suturing * Prior surgery in the operative eye * Prior corneal disease or ocular surface disease * With an inadequate follow-up within 7 days after surgery

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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

  • Peregrine Eye and Laser Institute

    Makati City, Philippines

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