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Clinical Trials/NCT02229669
NCT02229669
Completed
Not Applicable

Coronally Advanced Flap With Two Different Techniques for the Treatment of Multiple Gingival Recessions: A Split-mouth RCT

Paulista University0 sites10 target enrollmentMarch 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gingival Diseases
Sponsor
Paulista University
Enrollment
10
Primary Endpoint
Change from baseline in Marginal gingival recession to 6 months
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This study compared the clinical outcomes of coronally advanced flap using two different surgical strategies in the treatment of multiple gingival recessions.

Detailed Description

The objective of this split-mouth, randomized controlled trial was to compare the clinical outcomes of coronally advanced flap (CAF) using two different surgical strategies in the treatment of multiple gingival recessions. Recessions were randomly treated according to a split-mouth design by means of: CAF with oblique interdental incisions (OBL technique) or CAF with horizontal interdental incisions (HOR technique). Marginal gingival recession (REC), clinical attachment level (CAL), pocket probing depth (PPD), height of keratinized tissue (HKT) and thickness of keratinized tissue (TKT) were measured at baseline, 3 and 6 months after treatment. Patient-centered outcomes concerning morbidity and improvement in the esthetic appearance were recorded using a Visual Analogue Scale (VAS).

Registry
clinicaltrials.gov
Start Date
March 2011
End Date
July 2013
Last Updated
11 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Paulista University
Responsible Party
Principal Investigator
Principal Investigator

Guilherme Barrella

MS, DDS

Paulista University

Eligibility Criteria

Inclusion Criteria

  • Systemically healthy subjects
  • Patients should have bilateral Class I and II MGRs (Miller 1985) in maxillary tooth (at least three recession-type defects affecting adjacent teeth in each side of the maxilla).
  • At least 20 teeth and no sites with attachment loss and probing pocket depth (PPD) \> 3 mm.
  • Full-mouth plaque and bleeding on probing of \< 20%.
  • Involved tooth should present tooth vitality, absence of caries, restorations or extensive non-carious cervical lesion.

Exclusion Criteria

  • History of smoking.
  • Antimicrobial and anti-inflammatory therapies in the previous 2 months.
  • Previous mucogingival surgery at the region to be treated
  • Systemic conditions that could affect tissue healing (e.g. diabetes).
  • Use of orthodontic appliances.

Outcomes

Primary Outcomes

Change from baseline in Marginal gingival recession to 6 months

Time Frame: baseline, and at 3 and 6 months post-surgery

Secondary Outcomes

  • thickness of keratinized tissue(baseline, 3 and 6 months)
  • Probing deph(baseline, 3 and 6 months)
  • height of keratinized tissue(Baseline, 3 and 6 months)
  • Clinical attachment level(baseline, 3 and 6 months)

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