Comparison of two instruments in wisdom tooth removal
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Impacted lower third molars
- Registration Number
- CTRI/2018/04/013288
- Lead Sponsor
- ot applicable
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
1. All male and female patients with good general health condition.
2. ASA 1 and 2 patients.
3. Patients able and willing to give their own consent.
4. Patients willing for regular follow up.
Exclusion Criteria
1. Patients with acute infections at surgical site.
2. Patients unable to provide their own consent.
3. Patients with dense sclerotic bone of mandible.
Patients with systemic diseases or hematological conditions such as hemophilia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PainTimepoint: 3,7,14 days postoperative
- Secondary Outcome Measures
Name Time Method Swelling <br/ ><br>Trismus <br/ ><br>Paresthesia <br/ ><br>Time takenTimepoint: 3,7,14 days postoperative