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New bone graft technique may improve dental implant success

NCT ID NCT06867848

Disease control Sponsor: Nuhayra Ashour Muhammed 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This study tested two types of membranes (laminar bone and pericardium) combined with a sticky bone graft to improve bone quality for immediate dental implants. Twelve patients with a single hopeless front tooth received the treatment. The goal was to see if this approach helps implant stability and bone healing.

What this could mean

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

Active substance
laminar bone membrane and pericardium membrane with sticky bone graft
What this could lead to
If successful, this approach could improve bone quality and implant stability for people needing dental implants after tooth extraction.
What could go wrong
This is a very small, completed study with only 12 participants. Results may not apply to everyone, and long-term success is not yet proven.

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

12 people

The number who actually took part.

Started

Sep 2022

Finished

Apr 2025

Lead sponsor

A government agency

The lead sponsor is a government body.

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

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: * patient with a single hopeless tooth in maxillary anterior region. * sufficient bone apically and palatally * presence of natural contralateral tooth for the tooth being replaced * systemic healthy patients Exclusion Criteria: * extraction socket type III * acute infection in hopeless tooth * a heavy smoker patient * pregnant * had received chemotherapy or radiotherapy in previous year

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As listed by the trial registrant

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

The augmentation of labial defective wall in fresh extraction socket

Contacts and locations

Locations

  • Faculty of dental medicine for girls

    Cairo, Egypt