Comparison between Lignocaine HCL and Bupivacaine HCL local anesthetics when used as local application for pain control in mandibular third molar surgery
Not Applicable
- Conditions
- Health Condition 1: K011- Impacted teeth
- Registration Number
- CTRI/2024/04/065631
- Lead Sponsor
- Dr Ayushi Srivastava
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patient willing to participate in the study
within age group of 18-50
non smokers
moderately difficult pederson score 4-6
ASA status I
normal bleeding and clotting time
Exclusion Criteria
Patients who are not willing to participate in the study.
Patients with presence of any systemic disorders.
Patients with previous history of radiation therapy.
Patients who had undergone organ transplantation.
Patients allergic to anaesthetic agent.
Pregnant or lactating female subjects.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate and compare the postoperative pain on using Lignocaine HCL and Bupivacaine HCL soaked in Absorbable gelatin sponge when placed in the extraction socket after impacted mandibular third molar surgery. <br/ ><br>Postoperative pain will be measured using Visual Analogue Scale.Timepoint: Postoperative pain will be checked at following intervals postoperatively: <br/ ><br>4 hours <br/ ><br>8 hours <br/ ><br>12 hours <br/ ><br>1 day <br/ ><br>2 day <br/ ><br>3 day <br/ ><br>4 day <br/ ><br>5 day <br/ ><br>6 day <br/ ><br>7 day
- Secondary Outcome Measures
Name Time Method 1- to evaluate patients satisfaction score done using 5 point scale, 1- dissatisfied 2- rather dissastisfied 3- neither 4- rather satisfied 5- satisfied <br/ ><br>2-to evaluate analgesic rescue doses, reported back by the patient. <br/ ><br>3- to evaluate adverse effect like edema, trismus.Timepoint: Patient satisfaction towards postoperative pain will be checked at following intervals postoperatively: <br/ ><br>4 hours <br/ ><br>8 hours <br/ ><br>12 hours <br/ ><br>1 day <br/ ><br>2 day <br/ ><br>3 day <br/ ><br>4 day <br/ ><br>5 day <br/ ><br>6 day <br/ ><br>7 day <br/ ><br>adverse effect will be evaluated on post operative day 2 & day 7 <br/ ><br>resue analgesic dose will be checked on the 7th day postoperatively