to compare two methods of pain control in facial operations
Not Applicable
Completed
- Conditions
- Health Condition 1: null- 1. Age 18 to 60 years2. ASA I/II3. Scheduled for faciomaxillary surgery
- Registration Number
- CTRI/2017/05/008613
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1. Age 18 to 60 years
2. ASA I/II
3. Scheduled for faciomaxillary surgery
Exclusion Criteria
1.ASA III or more
2. Allergy to the drugs
3.Coagulopathy
4.Infection at puncture site
5.Mental disorder and Communication failure
6.Use of analgesia for premedication
7.Preexisting neurological disease like peripheral neuropathy
8.Patients plan for postop ventilation
9. polytrauma patient
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.additional fentanyl doses required intraoperativelyTimepoint: At the end of surgery
- Secondary Outcome Measures
Name Time Method 1. hemodynamics intraoperatively <br/ ><br>2. total analgesic dose in 24 hoursTimepoint: 1.at the end of surgery <br/ ><br>2. 24 hours postoperatively