To compare the efficacy of local pain relief drugs given by injection in the surgical woumd of locked jaw surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: M278- Other specified diseases of jawsHealth Condition 2: null- Patients with temporomandibular joint ankylosis
- Registration Number
- CTRI/2018/01/011160
- Lead Sponsor
- All India Institute of Medical Sciences New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 45
Inclusion Criteria
1.Patients above the age of 7 years
2.ASA physical status I-II
3.Scheduled for elective primary unilateral TMJ ankylosis surgeries
Exclusion Criteria
1.Patient refusal to participate in the study
2.History of allergy to any of the study drug
3.Patient on analgesic medication
4.Inability to comprehend VAS pain assessment scale
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To assess reduction in the total opioid consumption in the postoperative period over 24 hours. <br/ ><br> <br/ ><br>2.To assess reduction in the postoperative pain scores <br/ ><br>Timepoint: 1. post operative 0 hour, 2nd hour, 4th hour, 8th hour, 12th hour and 24th hour. <br/ ><br> <br/ ><br>2.post operative 0 hour, 2nd hour, 4th hour, 8th hour, 12th hour and 24th hour.
- Secondary Outcome Measures
Name Time Method 1. To assess the patient satisfaction level <br/ ><br>2. time to first rescue analgesic requirementTimepoint: 1. 24 hours