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Comparison of electrosurgery with surgical knife for incision in wisdom tooth surgery

Phase 4
Conditions
Health Condition 1: K011- Impacted teeth
Registration Number
CTRI/2023/08/056898
Lead Sponsor
Dr Kilari Anju Naidu
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Patient age group (18-40 years)

2.Patients with no relevant systemic disease (ASA Class 1)

Exclusion Criteria

1.Patient having electronic pacemaker

2.Patient with known history of bleeding or clotting disorders

3.Patients under radiotherapy or chemotherapy

4.Patients on immunosuppressive drugs

5.Patients with Diabetes mellitus

6.Patients with Hypertension

7.Pregnant patients

8.Intellectually and Developmentally Disabled patients

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To record incision time (Time from incision to elevation of mucoperiosteal flap )Timepoint: One intraoperatively
Secondary Outcome Measures
NameTimeMethod
1.To record bleeding from incision to elevation of mucoperiosteal flap <br/ ><br>2.To record odour perceived by the surgeon & patient during incision <br/ ><br>3.To record total time taken for procedure <br/ ><br>4.To record pain on first, third and seventh day after surgery <br/ ><br>5.To evaluate healing on first and fourth week after surgery <br/ ><br>Timepoint: Five time points Intraoperatively Bleeding, Odour, Total time taken <br/ ><br>Postoperative Pain on Day 1,Day 3 & Day 7 <br/ ><br>Postoperative healing on week 1 & week 4 <br/ ><br>
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