The comparison of Papilla preservation technique and pouch& tunnel with subepithelial connective tissue graft in dark triangle treatment
- Conditions
- Gingival recession.Gingival recession
- Registration Number
- IRCT201404071760N34
- Lead Sponsor
- Vice Chancellor for Research and Technology, Babol University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 10
existence the dark triangle anterior max; Tarnow all black triangles classified under group I, II; the selected teeth vital and no bleeding after probing; people over 18 years old; ability to maintain good oral hygiene (Oleary plaque score <20%); without stretching the frenum
Exclusion criteria: pregnancy; history of blood clotting problems, and hematologic; interfere with the healing agents (corticosteroids, anticancer); drugs interfering with platelet function (NSAIDS); smoking; any local or systemic disease with surgical procedures to prohibit administration; traumatic methods of brushing, toothbrush, toothpaste abrasives or harsh; long-term use of antibiotics in the previous quarter (more than 2 weeks); with known allergies to materials used in surgery; active infectious diseases (tuberculosis, hepatitis, HIV); use of drugs can lead to gingival enlargement.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Treatment of dark Triangle. Timepoint: Before surgery and three and six months after surgery. Method of measurement: Indexed Nordland and Tarnow.
- Secondary Outcome Measures
Name Time Method APico - coronal Papilla dimension. Timepoint: Before surgery and three and six months after surgery. Method of measurement: Mm.;MOD Papilla dimension. Timepoint: Before surgery and three and six months after surgery. Method of measurement: Mm.;Healing. Timepoint: Before surgery and three and six months after surgery. Method of measurement: Healing index.;Beauty. Timepoint: Before surgery and three and six months after surgery. Method of measurement: Indexed beauty VAS.