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

NCT ID: NCT01175720

Last Updated: 2011-11-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-08-31

Study Completion Date

2011-10-31

Brief Summary

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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

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Conditions

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Gingival Recession

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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test and control

The test and control technique will be tested in a split-mouth design.

Group Type EXPERIMENTAL

Periodontal surgery to gingival recessions

Intervention Type PROCEDURE

Test and control technique to treat gingival recessions.

Interventions

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Periodontal surgery to gingival recessions

Test and control technique to treat gingival recessions.

Intervention Type PROCEDURE

Eligibility Criteria

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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

* 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)
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Fundação de Amparo à Pesquisa do Estado de São Paulo

OTHER_GOV

Sponsor Role collaborator

University of Sao Paulo

OTHER

Sponsor Role lead

Responsible Party

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Arthur Belem Novaes Jr

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

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Arthur B. Novaes Júnior, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Sao Paulo

Lauro G. Ayub, MSD student

Role: PRINCIPAL_INVESTIGATOR

University of Sao Paulo

Locations

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Faculty of Dentistry of Ribeirão Preto USP

Ribeirão Preto, São Paulo, Brazil

Site Status

Countries

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Brazil

References

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Ayub LG, Ramos UD, Reino DM, Grisi MF, Taba M Jr, Souza SL, Palioto DB, Novaes AB Jr. A Randomized comparative clinical study of two surgical procedures to improve root coverage with the acellular dermal matrix graft. J Clin Periodontol. 2012 Sep;39(9):871-8. doi: 10.1111/j.1600-051X.2012.01915.x. Epub 2012 Jun 19.

Reference Type DERIVED
PMID: 22712624 (View on PubMed)

Other Identifiers

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lga030183

Identifier Type: -

Identifier Source: org_study_id