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Clinical Trials/NCT02248103
NCT02248103
Completed
Not Applicable

Comparison of Autogenous Periosteal Pedicle Graft and Collagen Membrane in Management of Periodontal Intrabony Defects: A Randomized Controlled Clinical Trial.

Cairo University0 sites20 target enrollmentMarch 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Periodontitis
Sponsor
Cairo University
Enrollment
20
Primary Endpoint
Clinical Attachment Level
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

A clinical and radiographic evaluation of autogenous periosteal pedicle graft in comparison with collagen membrane for management of periodontal intrabony defects.

Detailed Description

Twenty patients suffering from advanced chronic periodontitis were included in this randomized controlled clinical trial. Each subject contributed matched pairs of two- or three-walled intrabony defects. Each pair of periodontal defects were randomly assigned into the experimental group; periosteal pedicle graft guided tissue membrane or the positive control group; bioresorbable collagen guided tissue regeneration membrane. Clinical and radiographic parameters were recorded at baseline and at 6 months postoperatively.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
May 2014
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Noha Ayman Ghallab

Associate Professor of periodontology, faculty of oral and dental medicine

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Severe chronic periodontitis patients with at least two sites with pocket depth ≥ 6 mm and clinical attachment level ≥ 5 mm, with radiographic evidence of bone loss 2- or 3-wall intrabony defect depth ranging from 3 to 6 mm as detected in periapical radiographs
  • The facial surface of teeth adjacent to the interproximal defect should be free of extensive recession and marginal bone loss, with at least a 4 to 5 mm band of keratinized gingiva to allow for periosteal manipulation

Exclusion Criteria

  • Pregnant women
  • Subjects had \<22 permanent teeth
  • Having any given systemic disease
  • Taking any type of medication and/or antibiotic therapy during the 3 months before the study
  • Received periodontal treatment within the past 12 months
  • Current or former smokers

Outcomes

Primary Outcomes

Clinical Attachment Level

Time Frame: Baseline and 6 months

Estimation of clinical attachment level in chronic periodontitis patients at baseline and 6 months after guided tissue regeneration

Secondary Outcomes

  • Pocket Depth(Baseline and 6 months)
  • Bone Defect Area(Baseline and 6 months)

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