A clinical study to evaluate the postsurgical wound healing using different suture materials during gum surgeries
Not yet recruiting
- Conditions
- Chronic & Aggressive Periodontitis
- Registration Number
- CTRI/2018/04/013469
- Lead Sponsor
- Korukonda Radha Rani
- Brief Summary
The study is randomized controlled clinical trial to compare and clinically evaluate black silk (MERSILK),Polyglactin 910 (MONOCRYL), ePTFE (GORETEX) sutures during periodontal flap surgeries. The primary outcome is periodontal outcome which include reduction in probing pocket depth & gain in clinical attachment level recorded at 3 and 6 months. Secondary variables are proper handling of suture materials, early wound healing, assessment of pain, tissue reactivity at 7th day and 15th day.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
- Age: 20-65 years 2.
- Presence of atleast 2 or more teeth on each side of mouth with probing depth and clinical attachment level greater than 5mm.
- Systemically healthy patients with no contraindications for periodontal surgery.
Exclusion Criteria
- Pregnancy or lactating women 2.
- Uncontrolled systemic diseases.
- Consistent poor oral hygiene 4.Significant active caries.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Periodontal pocket elimination, Clinical attachment level gain Baseline, 1st month and 3rd month
- Secondary Outcome Measures
Name Time Method Suture handling characteristics Early wound healing, Pain scale and tissue reactions.
Trial Locations
- Locations (1)
Vishnu Dental College
🇮🇳Godavari, ANDHRA PRADESH, India
Vishnu Dental College🇮🇳Godavari, ANDHRA PRADESH, IndiaKorukonda Radha RaniPrincipal investigator9676461161radharani.k1993@gmail.com