Can a magnesium membrane preserve bone and gums better after tooth extraction?

NCT ID NCT07800377

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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
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 Results may not be published yet.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.
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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
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First seen Sep 02, 2026 · Last updated Sep 09, 2026 · Updated 3 times

Summary

This trial tests two membrane materials used during vestibular socket therapy, a technique for placing dental implants right after tooth extraction in the front of the mouth. Thirty adults who need such extractions will receive either a biodegradable magnesium membrane or a cortical lamina membrane, along with immediate implant placement and bone grafting. Researchers will compare changes in facial bone dimensions, soft tissue volume, implant stability, and aesthetic outcomes over six months. The goal is to see which material better preserves the bone and gum tissue needed for a successful, natural-looking implant.

What this could mean

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

Active substance
Vestibular Socket Therapy using a biodegradable magnesium membrane or a cortical lamina membrane, with immediate implant placement and bone grafting
What this could lead to
If it works, this could point toward a better way to preserve bone and gum tissue after tooth extraction, leading to more stable and natural-looking dental implants.
What could go wrong
This is a small, early-stage trial with only 30 participants, so results may not apply to everyone. The magnesium membrane is biodegradable and could break down too quickly or cause unexpected tissue reactions.

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.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Jun 2027

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 45 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: 1. Age between 18 and 45 years. 2. Requirement for extraction of one or more teeth in the maxillary esthetic zone with Type II extraction sockets. 3. Presence of adequate palatal and apical bone to achieve primary implant stability. 4. Adequate interocclusal restorative space for implant-supported prosthetic rehabilitation. 5. Good oral hygiene and satisfactory plaque control Exclusion Criteria: 1. Acute infection at the intended implant site (e.g., acute abscess or cellulitis). 2. Uncontrolled systemic diseases or medical conditions that may compromise bone healing or osseointegration. 3. History of irradiation to the head and neck region within one year before implant placement. 4. Alcohol or drug abuse. 5. Pregnancy or lactation. 6. Parafunctional habits such as bruxism or clenching. 7. Current smoking or tobacco using. 8. Poor oral hygiene or inability to maintain adequate plaque control.

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How to take part

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Contacts and locations

Locations

  • Outpatient Clinic of the Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Mansoura University

    Al Mansurah, Dakahlia Governorate, 35511, Egypt