Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
Healthy Volunteers
ID07492576

Evaluation of the Magnesium Shield Compared to Dual Zone Grafting Approach in Immediate Implant Site Management: A Randomized Controlled Clinical Trial

Led by British University In Egypt · Updated on 2026-04-01

22

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the use of a magnesium membrane compared to a dual zone grafting technique for managing immediate dental implant sites. This study focuses on patients with hopeless maxillary teeth and thin buccal bone plates, aiming to see which method better preserves bone volume, improves aesthetic outcomes, and reduces pain after implant placement. The trial assesses these approaches in terms of bone density, soft tissue contour, and patient comfort. The study compares two treatments: one uses a novel magnesium membrane placed between the soft tissue and buccal bone wall combined with inorganic bovine bone, and the other uses the dual zone concept where bone graft material fills both the bone and tissue zones around the implant. Both procedures involve atraumatic, flapless tooth extraction and immediate implant placement, followed by provisional restorations to support healing and maintain socket shape. Participants will undergo assessments before and after treatment at several time points up to 9 months, including measurements of ridge dimensions, pink esthetic scores, volumetric changes using digital scanning, mucosal recession, bone and soft tissue thickness, pain levels, and oral health indices. The trial includes safety monitoring and evaluates healing progress and implant site aesthetics over time. Total follow-up lasts 9 months after implant placement.

CONDITIONS

Brief Title

Evaluation of the Magnesium Shield Compared to Dual Zone Grafting Approach in Immediate Implant Site Management

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 60 years
  • Hopeless maxillary teeth with a thin buccal bone plate (1 mm or less) and intact soft tissue in the aesthetic zone
  • Periodontally healthy with good oral hygiene
  • Medically controlled patient
Not Eligible

You will not qualify if you...

  • Current smoker
  • Presence of systemic diseases
  • History of chemotherapy or radiotherapy within the past 2 years
  • Acute infection at the implant site

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Day 1

Participants undergo atraumatic flapless tooth extraction followed by immediate implant placement using either the magnesium shield device or the Dual Zone grafting technique. A provisional restoration is placed to seal the socket and maintain the architecture.

1 visit (in-person)

Post-operative Follow-up

Duration - 9 months

Participants are monitored for healing, pain, and implant site changes through clinical and imaging assessments.

Multiple visits at Day 3, 7, 14, 1 month, 3 months, 6 months, and 9 months (in-person)

Trial Site Locations

Total: 1 location

1

The British university in Egypt

Cairo, Egypt

Actively Recruiting

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Research Team

R

Rim M Ghanem, Bachelor degree of dentistry

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Comparison of a non-grafted socket shield technique with guided bone regeneration in immediate implant placement: a randomized clinical trial.

E Gurbuz, E Ceylan

https://pubmed.ncbi.nlm.nih.gov/39648089

Ridge alterations following implant placement in fresh extraction sockets: an experimental study in the dog.

Mauricio G Araújo, Flavia Sukekava, Jan L Wennström...

https://pubmed.ncbi.nlm.nih.gov/15882225