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Dental bone graft showdown: which material works best for implants?

NCT ID NCT07212985

Knowledge-focused Sponsor: Al-Azhar University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested two ways to rebuild jawbone for dental implants in 40 adults with narrow upper front jaws. One method used a block of bone from the chin mixed with cow-derived bone particles; the other used a synthetic material. Researchers measured bone width changes and complications over 6 months to see which approach worked better.

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

40 people

The number who actually took part.

Started

Jan 2023

Finished

Jun 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

18 years and older

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: * Adults ≥18 years requiring implant-supported restoration in the anterior maxilla Horizontal alveolar bone deficiency \<4 mm (Cawood \& Howell Class III-IV) Satisfactory oral hygiene No previous bone augmentation at study site Exclusion Criteria: * Uncontrolled systemic diseases History of head/neck irradiation or immunosuppression Oral lesions (e.g., lichen planus) Ongoing or recent IV bisphosphonate therapy Untreated periodontitis or poor oral hygiene Parafunctional habits, pregnancy, psychiatric disorders Recent tobacco use

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As listed by the trial registrant

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

Implant dentistry

Contacts and locations

Locations

  • Faculty of Oral and Dental Medicine, Nahda University,Taibah University

    Cairo, Egypt

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