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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
NameTimeMethod
Periodontal pocket elimination, Clinical attachment level gainBaseline, 1st month and 3rd month
Secondary Outcome Measures
NameTimeMethod
Suture handling characteristicsEarly wound healing, Pain scale and tissue reactions.

Trial Locations

Locations (1)

Vishnu Dental College

🇮🇳

Godavari, ANDHRA PRADESH, India

Vishnu Dental College
🇮🇳Godavari, ANDHRA PRADESH, India
Korukonda Radha Rani
Principal investigator
9676461161
radharani.k1993@gmail.com

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