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Clinical Comparison Between Two Surgical Techniques for the Treatment of Gingival Recessions

Not Applicable
Completed
Conditions
Gingival Recession
Interventions
Procedure: Periodontal surgery to gingival recessions
Registration Number
NCT01175720
Lead Sponsor
University of Sao Paulo
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
15
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
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Exclusion Criteria
  • Smokers
  • 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)
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
test and controlPeriodontal surgery to gingival recessionsThe test and control technique will be tested in a split-mouth design.
Primary Outcome Measures
NameTimeMethod
Percentage of root coverage6 months

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

Secondary Outcome Measures
NameTimeMethod
Keratinized Tissue6 months

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

Trial Locations

Locations (1)

Faculty of Dentistry of Ribeirão Preto USP

🇧🇷

Ribeirão Preto, São Paulo, Brazil

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