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Use of Perforated Barrier Membranes and IPRF Nano- Micro Sticky Bone

A

Ain Shams University

Status

Completed

Conditions

Bone Augmentation

Treatments

Procedure: Perforated collagen membrane
Procedure: Occlusive collagen membrane

Study type

Interventional

Funder types

Other

Identifiers

NCT04775940
FDASU-Rec ID021701

Details and patient eligibility

About

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 :

  1. clinical and Radiographic analysis .
  2. Histomorphometric analysis .

Enrollment

20 patients

Sex

All

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Healthy adult patients.
  2. 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

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

20 participants in 2 patient groups

Perforated collagen membrane
Experimental group
Treatment:
Procedure: Perforated collagen membrane
Occlusive collagen membrane
Active Comparator group
Treatment:
Procedure: Occlusive collagen membrane

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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