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Clinical Trials/NCT02916186
NCT02916186
Unknown
Not Applicable

Evaluation of Subepithelial Connective Tissue Graft Versus Acellular Dermal Matrix With Tunnel Technique in Treatment of Multiple Gingival Recessions (Randomized Clinical Trial, Parallel Design)

Cairo University0 sites68 target enrollmentOctober 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gingival Recession
Sponsor
Cairo University
Enrollment
68
Primary Endpoint
patient Satisfaction .
Last Updated
9 years ago

Overview

Brief Summary

The goal of the present study is to compare the amount of root coverage resulting from subepithelial connective tissue graft and acellular dermal matrix associated with tunnel technique among patients suffering from multiple gingival recession.

Detailed Description

Acellular dermal matrix with Tunnel technique will offers great advantages for patients with multiple gingival recession as regards decrease surgical time, Post-Operative pain and root coverage, clinical attachment level, width of Keratinized gingiva, gingival biotype compared to subepithelial connective tissue graft with Tunnel technique.

Registry
clinicaltrials.gov
Start Date
October 2016
End Date
September 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Fatema Mohammed Ali Elmahdi

Dr

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Subjects with facial multiple gingival recession defects classified as either class I or II defects according to Miller's classification (Miller 1985).
  • Subjects aged between 18 - 60 years old.
  • Patients should be free from any systemic disease that may affect normal healing of tissue, and predictable outcome.
  • Patients with good oral hygiene.

Exclusion Criteria

  • Current and former smokers.
  • Pregnant females.
  • Subjects received any periodontal therapy for minimum of 6 months prior to the study.
  • Subjects taking drugs known to interfere with wound healing.
  • Subjects with unacceptable oral hygiene with plaque index \>
  • Teeth with non-carious cervical lesions (NCCL), cervical caries and malalignment.

Outcomes

Primary Outcomes

patient Satisfaction .

Time Frame: 1 year

measured by VAS scale

Secondary Outcomes

  • root coverage(1 year)
  • Gingival Bio-type(1 year)
  • Width of Keratinized Tissue(1 year)
  • Clinical Attachment Level(1 year)

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