A clinical study to evaluate the workingof silk sutures and barbed sutures as wound closure agent after third molar surgery.
Phase 1
- Conditions
- Health Condition 1: K011- Impacted teeth
- Registration Number
- CTRI/2023/06/054263
- Lead Sponsor
- Dr Nandini Mahesh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients who fall within the ASA 1 (American Society of Anaesthesiology) classification
Patients with clinical and radiological records indicating that bilaterally impacted mandibular third molars require surgical removal.
Patients with similar difficulty indexes of impacted mandibular teeth
Exclusion Criteria
Pregnant and lactating women.
Patients with history of systemic diseases
Patients with bleeding disorder.
Patient who has lignocaine allergy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To measure duration of time taken for closure of the intraoral wound.Timepoint: During surgery in minutes
- Secondary Outcome Measures
Name Time Method To measure the amount of post operative swelling .Timepoint: On 3rd & 7th postoperative day <br/ ><br>The following measurements were made between five landmarks <br/ ><br> Gonion to lateral canthus of eye. <br/ ><br> Tragus to angle of mouth. <br/ ><br> Tragus to pogonion. <br/ ><br>;Wound healingTimepoint: Using Early Wound Healing Score