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New pinhole gum surgery could reduce pain and improve smiles

NCT ID NCT07162207

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests a modified pinhole surgical technique for treating localized gum recession. It compares using a bi-layer collagen membrane versus a connective tissue graft to cover exposed tooth roots. The trial involves 18 healthy adults with gum recession and will measure changes in gum depth, width, thickness, and patient satisfaction over 6 months.

What this could mean

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

Active substance
Bi-layer collagen membrane or connective tissue graft
What this could lead to
If successful, this could offer a less invasive, equally effective option for covering exposed tooth roots, reducing pain and improving gum appearance.
What could go wrong
This is a very small, early-stage trial with only 18 patients, so results may not apply to everyone. The collagen membrane may not work as well as the standard graft, and long-term outcomes are unknown.

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

18 people

The number who actually took part.

Started

Jun 2024

Expected to finish

Dec 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 years and older

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: 1. Patients have ages above 18 years. 2. Patients included in the study are classified with Cairo RT1 and RT2 localized recession defect Cairo et al. (2011). 3. Patients have at least 1 mm of residual keratinized tissue. 4. Recession depth ≥ 2mm. 5. Recession is not caused by periodontal disease. 6. Patients have good oral hygiene. Exclusion Criteria: 1. Patients with systemic diseases. 2. Pregnant and lactating women. 3. Smoking patients and drug abusers. 4. Patients with mal-positioned and rotated teeth. 5. Patients with periodontally affected teeth adjacent to the treated sites. 6. Patients having carious lesions or restorations in the treated teeth.

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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

  • Faculty of Dentistry- Ain Shams University

    Cairo, Egypt

More trials for these conditions

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