Two Types of PRF Membranes in Management of Dehiscence Defect in Posterior Mandible

NCT ID: NCT07164417

Last Updated: 2025-09-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-12

Study Completion Date

2025-01-20

Brief Summary

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Background: Placement of implants in an atrophic posterior ridge is a challenge for so many clinicians. The success of dental implants depends on the volume of alveolar bone available to provide stability. Bone grafting using xenograft with PRF and e-PRF as a membrane has shown promising results in both bone healing and defect reconstruction. Aim of the study: to evaluate the effect of Platelet-rich fibrin (PRF) and Extended Platelet-rich fibrin (e-PRF) as a membrane with xenograft to increase the width of ridge in posterior mandible with simultaneous implant placement.

Detailed Description

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Conditions

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Atrophic Mandible

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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PRF

Group Type ACTIVE_COMPARATOR

PRF membrane will be used with xenograft simultaneously with implant placement

Intervention Type OTHER

Peripheral blood is collected in 9-10 mL additive-free tubes and centrifuged horizontally at 700-2000 g for 8 minutes.

e-PRF

Group Type EXPERIMENTAL

e-PRF membrane will be used with xenograft simultaneously with implant placement.

Intervention Type OTHER

Peripheral blood is collected in plain tubes and centrifuged (700-2000 g, 8 min) to separate plasma from red cells. The first 2-4 mL of platelet-poor plasma (PPP) is withdrawn and heated at 75 °C for 10 minutes to form albumin gel, then cooled for 1-2 minutes. Meanwhile, the remaining blood fractions (buffy coat, liquid PRF, red cells) are kept cooled to prevent premature clotting.

Interventions

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e-PRF membrane will be used with xenograft simultaneously with implant placement.

Peripheral blood is collected in plain tubes and centrifuged (700-2000 g, 8 min) to separate plasma from red cells. The first 2-4 mL of platelet-poor plasma (PPP) is withdrawn and heated at 75 °C for 10 minutes to form albumin gel, then cooled for 1-2 minutes. Meanwhile, the remaining blood fractions (buffy coat, liquid PRF, red cells) are kept cooled to prevent premature clotting.

Intervention Type OTHER

PRF membrane will be used with xenograft simultaneously with implant placement

Peripheral blood is collected in 9-10 mL additive-free tubes and centrifuged horizontally at 700-2000 g for 8 minutes.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient with one or more missing posterior mandibular teeth.
* Patient with atrophic posterior mandible with residual ridge width in the range of 4 to 6mm.
* Patient with good oral hygiene and acceptable inter-arch space less than or equal to the restoration

Exclusion Criteria

* The patient underwent alveolar ridge reconstruction in the same area.
* Patients with immune diseases, uncontrolled hypertension, and uncontrolled diabetes.
* Patient with any pathological condition at the site of surgery.
* Heavy smoker, alcohol abuse, parafunctional habits.
Minimum Eligible Age

20 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Alexandria University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Outpatient Clinic of Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Alexandria University, Egypt

Alexandria, Azarita, Egypt

Site Status

Countries

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Egypt

Other Identifiers

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0936-06/2024

Identifier Type: -

Identifier Source: org_study_id

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