Extended Platelet Rich Fibrin in Mandibular Alveolar Ridge Splitting

NCT ID: NCT06637982

Last Updated: 2024-10-15

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 32 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-10-10
• Study Completion Date: 2025-10-10

Brief Summary

Thirty two healthy implants will be selected from the outpatient clinic of the oral and maxillofacial department of Mansoura university to be included in this study for replacement of lost posterior teeth with limited bone width.

Conditions

Ridge Splitting

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

ridge splitting with allograft and pericardium membrane

Group Type: EXPERIMENTAL

ridge splitting with the use of allograft and pericardium membrane

Intervention Type: PROCEDURE

ridge splitting with the use of allograft and pericardium membrane

ridge splitting with extended platelet rich fibrin

Group Type: EXPERIMENTAL

ridge splitting with the use of extended platelet rich fibrin

Intervention Type: PROCEDURE

ridge splitting with the use of extended platelet rich fibrin

Interventions

ridge splitting with the use of allograft and pericardium membrane

ridge splitting with the use of allograft and pericardium membrane

Intervention Type: PROCEDURE

ridge splitting with the use of extended platelet rich fibrin

ridge splitting with the use of extended platelet rich fibrin

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Patient age 18 years old and older.
• Patient's cooperation, motivation and good oral hygiene.
• Atrophic posterior mandible of horizontal alveolar dimension range between 3 - 6 mm at the crest, with minimum 10 mm vertical height from the alveolar crest to the superior border of the inferior alveolar canal.
• Absence of undercuts in buccal aspect of the ridge.
• Favorable occlusion and no parafunctional habits.
• Patients able to comply with the required recall visits.
• No gender preface in selection of the patients.
• Acceptable inter-arch space for the future prosthesis.

Exclusion Criteria

• Any pathological condition at the site of surgery.
• Patients with systemic diseases that contra-indicate the surgical procedure such as uncontrolled diabetes mellitus, bleeding disorders, serious osseous disorders, and mental disorders.
• Patient taking drugs that could affect bone healing process as immunosuppressive drugs and bisphosphonates.
• Heavy smoking and alcoholism.
• Parafunctional habits such as bruxism and clenching.
• Signs of acute infection or pus discharge.
• Untreated periodontal disease or bad oral hygiene.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Mansoura University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Mansoura University

Mansoura, Egypt, , Egypt

Countries

Egypt

Central Contacts

faisal alshammri

Role: CONTACT

fasialshammry@std.mans.edu.eg

1555250898 ext. 0020

Facility Contacts

faisal alshammri

Role: primary

Other Identifiers

A0302024OS

Identifier Type: -

Identifier Source: org_study_id