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Gum graft recovery boosted by natural gels?

NCT ID NCT06867055

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 adding a natural gel made from your own blood (I-PRF) or a hyaluronic acid gel to a standard sponge helps the roof of the mouth heal faster after a gum graft. 67 healthy adults took part. Results suggest these gels may speed healing and reduce pain and burning after surgery.

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

67 people

The number who actually took part.

Started

May 2023

Finished

Sep 2025

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 58 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: * Inclusion criteria for the study were; * patients older than 18 and * systemically healthy patients, * who didn't use drugs that affect wound healing, * didn't have coagulation disorder and nausea, and * were not anti-inflammatory drug allergy sufferers. Exclusion Criteria: * Exclusion criteria for the study were; * patients who had systematic disorders (such as diabetes, hypertension, radiotherapy, chemotherapy), * patients who were former or active smokers and alcohol users, * pregnant and breastfeeding, lactation, menstruation, * patients with poor oral hygiene, and patients who didn't attend regular check-ups.

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Health Sciences University Gulhane Faculty of Dentistry

    Ankara, Ankara, (533) 316-1232, Turkey (Türkiye)

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