To study the effect of lornoxicam drug given before removal of the lower wisdom tooth
Not Applicable
- Conditions
- Health Condition 1: K011- Impacted teeth
- Registration Number
- CTRI/2020/09/027822
- Lead Sponsor
- Dr Bonthu Vineela
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients between 18-28 years
2.Patients willing to give informed consent
3.Patients with bilaterally symmetrical impacted mandibular third molars
4.Patients with ASA Class 1 and 2
Exclusion Criteria
1.Patients not willing to give informed consent
2.Patient having inflammation or infection at the site of surgery
3.Patients allergic to any NSAIDS & patients who took NSAIDs 72 hours prior to surgery
4.Patients under Warfarin and Digoxin use
5.Patients with cardiac, renal and hepatic insufficiency
6.Patients with gastrointestinal disturbances
7.Pregnant and lactating women
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Pain measured on the VAS scale at 1st 2nd 4th 6th 8th & 12th hour postoperatively <br/ ><br>2.The first incidence of pain postoperatively <br/ ><br>3.Number of Rescue analgesics consumed within 24 hours postoperatively (in a period of 8 hours gap )Timepoint: 1.Pain measured on the VAS scale at 1st 2nd 4th 6th 8th & 12th hour postoperatively <br/ ><br>2.Number of Rescue analgesics consumed within 24 hours postoperatively (in a period of 8 hours gap )
- Secondary Outcome Measures
Name Time Method 1.The first incidence of pain postoperatively at 1st 2nd 4th 6th 8th & 12th-hour postoperativelyTimepoint: 1.The first incidence of pain postoperatively at 1st 2nd 4th 6th 8th & 12th-hour postoperatively