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Clinical Trials/NCT01175720
NCT01175720
Completed
Not Applicable

Clinical Comparison Between Two Surgical Techniques With Acellular Dermal Matrix Graft in the Treatment of Gingival Recessions

University of Sao Paulo1 site in 1 country15 target enrollmentAugust 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gingival Recession
Sponsor
University of Sao Paulo
Enrollment
15
Locations
1
Primary Endpoint
Percentage of root coverage
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The aim of this study is to test a surgical technique for the treatment of gingival recessions. The hypothesis of the study is to promote greater root coverage and better healing.

Registry
clinicaltrials.gov
Start Date
August 2010
End Date
October 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Arthur Belem Novaes Jr

Clinical comparison between two surgical techniques with acellular dermal matrix graft in the treatment of gingival recessions

University of Sao Paulo

Eligibility Criteria

Inclusion Criteria

  • Recession defects are Miller's class I or II and do not vary more or equal than 3 mm
  • Main complaint aesthetic issues or dentine hypersensitivity
  • The patient must be a candidate for bilateral root coverage procedure
  • Patient shows sufficient plaque control (FMPS \< 20%)
  • The patient is able to comply with the study-related procedures such as exercising good oral hygiene and attending all follow-up procedures
  • The patient is able to fully understand the nature of the proposed surgery and is able to provide a signed informed consent

Exclusion Criteria

  • Systemic diseases
  • Pregnants or lactating
  • Periodontal disease
  • General contraindications for dental and/or surgical treatment are present
  • The patient has a history of malignancy, radiotherapy, or chemotherapy for malignancy within the past five years
  • The patient is taking medications or having treatments which have an effect on mucosal healing in general (e.g. steroids, large doses of anti-inflammatory drugs)

Outcomes

Primary Outcomes

Percentage of root coverage

Time Frame: 6 months

Clinical parameters will be assessed after 6 months of surgical procedures.

Secondary Outcomes

  • Keratinized Tissue(6 months)

Study Sites (1)

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