Gingival Recession Clinical Trial
Official title:
A New Regenerative Therapeutic Approach for Root Coverage: a Randomized Clinical Trial
Verified date | June 2012 |
Source | University of Sao Paulo |
Contact | n/a |
Is FDA regulated | No |
Health authority | Brazil: Ministry of Health |
Study type | Interventional |
Different surgical techniques have been proposed for root coverage, showing varying results especially in areas of deep recessions. The aim of this study is to evaluate the effectiveness of the newly forming bone technique (NFB)as an alternative treatment for Miller class I or II deep recessions, requiring regeneration of lost periodontal tissues. Sample should be comprised of patients aged 18-45 years, both genders, presenting at least one site with marginal tissue recession >4mm. Patients will be randomly assigned to either one of the groups, based on treatment technique: newly forming bone (NFB) or subepithelial connective tissue graft (SCTG). Clinical examinations will be performed by a single blinded examiner at baseline, 1, 3, 6 and 9 months after surgery. Intra-group analysis will be performed by one way analysis of variance for repeated measures. Inter-group analysis will be performed by unpaired t-test for each of evaluation periods.
Status | Completed |
Enrollment | 15 |
Est. completion date | February 2009 |
Est. primary completion date | November 2008 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Healthy adults with at least one tooth presenting marginal tissue recession equal to or greater than 4mm in depth and one edentulous area or tooth to be extracted. Exclusion Criteria: - Smokers - Pregnants - Use of anti-convulsants, anti-hypertensives, cyclosporine or hormones - Use of antibiotics for the last 6 months - Patients under treatment for medical conditions or presenting systemic disorders that would impair treatment results (e.g.: uncontrolled diabetes mellitus) |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Brazil | School of Dentistry at Bauru-USP, Discipline of Periodontics | Bauru | SP |
Lead Sponsor | Collaborator |
---|---|
University of Sao Paulo | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior. |
Brazil,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percentage of Root Coverage | Percentage of root coverage determined by: [area covered]/[total area to be covered] x 100 (in %) | Baseline, 9 months post-operatively | No |
Secondary | Gain of Clinical Attachment Level | Investigation of clinical attachment level, probing depth and reduction of recession depth | 9 months post-operatively | No |
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