The Use of Perforated Barrier Membranes and IPRF Nano- Micro Sticky Bone in Horizontal Alveolar Ridge Augmentation - Controlled Clinical and Histomorphometric Study

Ain Shams University1 site in 1 country20 target enrollmentMarch 1, 2018

ConditionsBone Augmentation

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Bone Augmentation
Sponsor: Ain Shams University
Enrollment: 20
Locations: 1
Primary Endpoint: Horizontal alveolar bone width in mm
Status: Completed
Last Updated: 5 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

Comparing amount of horizontal bone gain 4 months after alveolar ridge augmentation using IPRF Nano- micro Sticky Bone with perforated collagen membrane versus occlusive barrier membrane by :

clinical and Radiographic analysis .
Histomorphometric analysis .

Registry

clinicaltrials.gov

Start Date

March 1, 2018

End Date

December 1, 2019

Last Updated

5 years ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

Ain Shams University

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Healthy adult patients.
•Both sex, males and females. 3-Age from 20 - 40 years old. 4-All patients will be free from any systemic diseases as evidenced by Burkett's oral medicine health history questionnaire.
•5-Remaining alveolar bone ≥ 8mm vertically and ≤ 4 mm horizontally. 6-Gingival biotype 1-2mm thickness.

Exclusion Criteria

•Pregnant and breast feeding females.
•Mentally retarded Patients.
•Presence of hematologic disease.
•Previous radiation, chemotherapy, or immunosuppressive treatments.
•Diabetes mellitus, metabolic bone disease, ongoing treatment with bisphosphonates drugs, or pregnancy.
•Anticoagulant drugs, Endocarditis risk factors, renal and hepatic failure