Coronally Advanced Flap With Two Different Techniques for the Treatment of Multiple Gingival Recessions

Not Applicable

Completed

• Conditions: Gingival Diseases

• Registration Number: NCT02229669
• Lead Sponsor: Paulista University

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).

Study Timeline

• Study Start: 2011-03
• Primary Completion: 2012-08
• Study Completion: 2013-07
• Status Verified: 2014-08
• Study First Submitted: 2014-08-21
• Study First Submitted QC: 2014-08-28
• Last Update Submitted: 2014-08-28
• Study First Posted: 2014-09-01
• Last Update Posted: 2014-09-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 10

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Primary Outcome Measures

Name	Time	Method
Change from baseline in Marginal gingival recession to 6 months	baseline, and at 3 and 6 months post-surgery

Secondary Outcome Measures

Name	Time	Method
thickness of keratinized tissue	baseline, 3 and 6 months
Probing deph	baseline, 3 and 6 months
Clinical attachment level	baseline, 3 and 6 months
height of keratinized tissue	Baseline, 3 and 6 months