Comparision of Two Different Surgical Techniques with Blood Derivatives for Treatment of Maxillary Gingival Recession- A Randomized Controlled Study
Phase 3
Completed
- Conditions
- Health Condition 1: K060- Gingival recession
- Registration Number
- CTRI/2022/06/043380
- Lead Sponsor
- Dr Megha Poojari
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
Men or Women between 18 and 60 years of age.
Cairo et al RT1 gingival recession defects measuring = 2mm anterior teeth or premolars, on contralateral sides of same arch or one in each quadrant, with complaint of sensitive teeth or esthetic concerns.
Vital teeth, free of faulty restorations.
Patients who gave informed consent for the study.
Exclusion Criteria
History of smoking or tabacco consumption.
Pregnant or lactating women.
Patient with active periodontal disease.
History of surgical treatment in the delineated area for atleast 2 years prior to the study.
Patients with systemic condition that contraindicate surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Significant improvement in clinical parameters:pocket probing depth,clinical attachment level,thickness of attached gingiva,width of keratinized tissue,gingival recession width, vertical depth of recession and percentage root coverage.Timepoint: Baseline, 1 week, 2 weeks, 1 month and 3 months.
- Secondary Outcome Measures
Name Time Method better patient pain comfortTimepoint: 1 week