A study to compare the efficacy of standard medications and a new protocol of medications proposed after wisdom tooth removal.
Not Applicable
- Conditions
- Health Condition 1: K011- Impacted teeth
- Registration Number
- CTRI/2023/03/050411
- Lead Sponsor
- Adarsh Kudva
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Age: 18 years or older
2) Bilateral impacted lower third molar needing extraction with the necessity of bone removal based on panoramic radiography.
3) Patient reporting for prophylactic removal of mandibular 3rd molar.
4) Patients with no active infection.
Exclusion Criteria
1) Patients with associated pathologies like cysts or tumors of the jaw bones.
2) Systemic illness and inflammation.
3) Pre-existing infection at the extraction site
4) Patients with history of GI or allergic co-morbidities.
5) Pregnant women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Pain based on the VAS Scale. <br/ ><br>2. Swelling/ Edema as perceived by the patient. <br/ ><br>3. Surgical site infection. <br/ ><br>4. Signs of infection. <br/ ><br>5. Restriction in mouth opening. <br/ ><br>6. Formation of alveolar osteitis.Timepoint: Post-operative day 0 and post-operative day 5
- Secondary Outcome Measures
Name Time Method ATimepoint: NA