Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Simple stitch before gum surgery may cut bleeding and pain

NCT ID NCT05395923

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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether placing stitches (pre-sutures) in the roof of the mouth before taking a gum graft can reduce bleeding and pain. 32 adults with gum recession took part. Researchers measured blood loss, pain, and healing after surgery. The goal was to see if this simple step improves patient comfort and recovery.

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

32 people

The number who actually took part.

Started

Jan 2023

Finished

Jul 2024

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

19 to 60 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * \- The patient must be over the age of 18, * Not having any systemic disease, * Not receiving chemotherapy or radiotherapy treatment, * Not using drugs regularly and not being addicted to drugs, * Not be in pregnancy and/or lactation period, * Not smoking, * Not having received antibiotic treatment in the last 6 months, * Presence of Cairo Type 1 or Type 2 recession defect in a single tooth, * The patient is cooperative. Exclusion Criteria: * The patient is younger than 18 years old, * Active infectious disease (acute hepatitis, AIDS, tuberculosis), cancer or any systemic condition that may affect periodontal tissues, * Receiving chemotherapy or radiotherapy treatment, * Being on regular medication and being addicted to drugs, * Patients with a plaque score greater than 20% after phase I treatment (Silness and Löe, 1964), * Being in pregnancy and/or lactation period, * Being a smoker * To have been treated with antibiotics in the last 6 months, * Not being cooperative.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Bleeding hemorrhage are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

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

  • Biruni University

    Istanbul, Zeytinburnu, Turkey (Türkiye)

More trials for these conditions

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