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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02229669
Other study ID # U1111-1158-9611
Secondary ID
Status Completed
Phase N/A
First received August 21, 2014
Last updated August 28, 2014
Start date March 2011
Est. completion date July 2013

Study information

Verified date August 2014
Source Paulista University
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

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


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).


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date July 2013
Est. primary completion date August 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility 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

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Intervention

Procedure:
Horizontal incisions
Performed by using horizontal interdental incisions. An initial horizontal incision was made slightly coronal to the CEJ from the distal to the mesial papilla of the teeth with the recessions. A second incision, 1 to 2 mm apart and parallel to the first incision, was made apically. A sulcular incision was made to link the second incisions and the blade was inserted (2 to 3 mm) extending beyond the mucogingival junction (MGJ), to create a uniform split-thickness flap. The tissue between the two incisions was partially removed to obtain a uniform receptor site that permitted primary closure. Approximation sutures to place the edge of the flap at the base of the remaining papilla were performed. Passive closure of the wound margins without tension was achieved with interrupted coaptation.
Oblique incisions
Coronally advanced flap was performed by using oblique incisions in interdental areas, according to the technique proposed by Zucchelli & De Sanctis (2000). Oblique submarginal interdental incisions were performed and continued with the intrasulcular incisions at the recession defects, resulting in a envelop flap that was raised with a split-full-split approach in the coronal-apical direction. During coronal advancement, each surgical papilla was dislocated with respect to the de-epithelized anatomic papilla by the oblique incisions. Interrupted sutures were performed to stabilize single surgical papilla over the interdental connective tissue bed.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Paulista University

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in Marginal gingival recession to 6 months baseline, and at 3 and 6 months post-surgery Yes
Secondary height of keratinized tissue Baseline, 3 and 6 months Yes
Secondary thickness of keratinized tissue baseline, 3 and 6 months Yes
Secondary Clinical attachment level baseline, 3 and 6 months Yes
Secondary Probing deph baseline, 3 and 6 months Yes
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