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Stitches or glue? small study tests better way to close mouth cuts

NCT ID NCT07491276

Symptom relief Sponsor: Future University in Egypt Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 This study
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests two newer ways to close cuts inside the mouth after removing a damaged tooth: special self-anchoring stitches and a medical glue. Thirty adults will be randomly assigned to one of these methods or to standard stitches. The goal is to see which approach is faster, causes less pain, and leads to better healing.

What this could mean

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

Active substance
PDO Knotless Barbed Suture, N-Butyl Cyanoacrylate Glue (PERIACRYL), 3/0 Resorbable PGA Suture
What this could lead to
If one method works better, it could mean less pain and faster healing after oral surgery.
What could go wrong
This is a small, early-stage study with only 30 people, so results may not apply to everyone. Both methods are already used, so no big breakthrough is expected.

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

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2025

Expected to finish

May 2026

An estimate. End dates often move.

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

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: * Patients requiring Intra-oral wound closure following intra-oral incisions after surgical extraction of non-restorable teeth. * Good oral hygiene. * Highly motivated patients * Patients agreed to follow-up for post-operative evaluation with informed consent * Age between 18- 50 years old * Both genders: Males \& Females Exclusion Criteria: * Medically compromised patients as uncontrolled Diabetes, uncontrolled hypertension. * Patients on chemotherapy or radiation. * Patients with bad oral hygiene . * Uncooperative patients: mentally retarded patients. * Heavy smokers. ( \> 1 pack/day).

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Intraoral surgical incisions Non-restorable teeth Surgical tooth extraction Wound closure

Contacts and locations

Locations

  • Faculty of Oral and Dental Medicine, Future University in Egypt

    New Cairo, Cairo Governorate, 11835, Egypt

More trials for these conditions

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