Testing analgesic efficiency of two medications in orthopaedic surgeries.
- Conditions
- Health Condition 1: null- The study was conducted in 100 ASA physical status grade I and II, of either sex, between the age group of 18-65 years scheduled for elective upper limb orthopedic surgeries
- Registration Number
- CTRI/2017/07/009049
- Lead Sponsor
- St Stephens Hospital committee
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
The study was conducted in 100 ASA physical status grade I and II, of either sex, between the age group of 18-65 years scheduled for elective upper limb orthopedic surgeries under general anesthesia (GA). Patients were admitted at least 24 hours before surgery. Detailed history, examination and relevant investigations like complete blood count, renal/liver function tests, coagulation profile, X-ray chest and ECG were carried out. Patients posted for unilateral or bilateral upper limb surgery e.g., shoulder, humerus and elbow surgery were included
Patients allergic reaction to study drugs, gastric ulcer complaints for last 6 months, coagulopathy, alcohol or drug addicts, neurological or psychiatric illness and clinically significant major organ disease were excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pulse rate, blood pressure, and oxygen saturation were recorded intraoperatively and after extubation. <br/ ><br>Intraoperative pain was assessed by hemodynamic parameters (inadvertent rise in HR, BP) while postoperative pain assessment using visual analog score (VAS) ranging from 0-100 mm was done postoperative complication was noted and treated accordingly. <br/ ><br>Timepoint: Pulse rate, blood pressure, and oxygen saturation were recorded 5 minutes before induction and every 10 minutes intraoperatively and after extubation. <br/ ><br>Intraoperative pain was assessed by hemodynamic parameters (inadvertent rise in HR, BP) while postoperative pain assessment using visual analog score (VAS) ranging from 0-100 mm was done postoperative complication was noted and treated accordingly. <br/ ><br>
- Secondary Outcome Measures
Name Time Method any postoperative complication was noted and treated accordingly.Timepoint: AFTER EXTUBATION (GA).at 15 min, 30min, 1 hr, 2hrs, 4hrs and 6hrs