A study to compare the effect of pain releif among two drugs in elective oral surgery
Phase 2
Completed
- Conditions
- Health Condition 1: null- Healthy patients only
- Registration Number
- CTRI/2017/08/009468
- Lead Sponsor
- JIPMER PUDUCHERRY
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 64
Inclusion Criteria
Healthy patients in above age groups for elective maxillofacial surgery
Exclusion Criteria
Known Heart disease , allergy to drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time for request of first analgesic after surgeryTimepoint: Time from extubation to onset of pain( e.g. If patient is extubated at 10 AM and the onset of pain is 11 AM, then the time for request of first analgesic dose is 1 hour )
- Secondary Outcome Measures
Name Time Method Intra-operative supplemental analgesic requirementTimepoint: Cumulative doses of supplemental analgesics given during the intra-operative period in addition to the drugs being compared(In my study Fentanyl.. Hence specific time points is not applicable.