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Clinical Trials/NCT01901822
NCT01901822
Completed
Not Applicable

Root Coverage With Acellular Dermal Matrix Using the Coronally Positioned Tunnel Technique Comparing Two Different Suturing Techniques.

University of Louisville1 site in 1 country16 target enrollmentSeptember 2013
ConditionsRoot Coverage

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Root Coverage
Sponsor
University of Louisville
Enrollment
16
Locations
1
Primary Endpoint
Percent root coverage
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The hypothesis of this study is that coronally positioned tunnel with acellular dermal matrix using a continuous sling suture to secure both the graft and the flap will result in better percent root coverage compared to the continuous sling suturing technique to secure the graft and the flap separately.

Detailed Description

Thirty patients will be selected by meeting the following criteria: Inclusion Criteria: A. At least one Miller Class I or II mucogingival defect ≥ 3 mm (Miller 1985). B. The mucogingival defect must be on a non-molar tooth. C. Patients must be between ≥ 18 years of age. Exclusion Criteria: A. Patients with debilitating systemic or diseases that significantly affect the periodontium. B. Patients with a known allergy to any of the materials that will be used in the study, including systemic antibiotics (tetracycline and doxycycline). C. Patients requiring antibiotic prophylaxis. D. Root surface restorations at the site of recession. E. No detectable cemento-enamel junction. F. Patients who fail to maintain oral hygiene levels of at least 80% plaque free surfaces. G. Patients who are pregnant or lactating. H. Patients who use tobacco products (smoking or smokeless tobacco). I. Patients with alcohol abuse problems. J. Patients undergoing long-term steroid therapy. K. History of previous root coverage procedures, graft or guided tissue regeneration, on the test teeth. L. Patients who fail to complete the informed consent form.

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

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Henry Greenwell

Professor

University of Louisville

Eligibility Criteria

Inclusion Criteria

  • At least one Miller Class I or II mucogingival defect ≥ 3 mm (Miller 1985).
  • The mucogingival defect must be on a non-molar tooth.
  • Patients must be between ≥ 18 years of age.

Exclusion Criteria

  • Patients with a known allergy to any of the materials that will be used in the study, including systemic antibiotics (tetracycline and doxycycline).
  • Patients requiring antibiotic prophylaxis.
  • Root surface restorations at the site of recession.
  • No detectable cemento-enamel junction.
  • Patients who fail to maintain oral hygiene levels of at least 80% plaque free surfaces.
  • Patients who are pregnant or lactating.
  • Patients who use tobacco products (smoking or smokeless tobacco).
  • Patients with alcohol abuse problems.
  • Patients undergoing long-term steroid therapy.
  • History of previous root coverage procedures, graft or guided tissue regeneration, on the test teeth.

Outcomes

Primary Outcomes

Percent root coverage

Time Frame: 6 months

The amount of root coverage will be measured and converted to a percent.

Study Sites (1)

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