A study to compare Fentanyl and Butorphanol as adjuvant drugs to local anesthetics in combined spinal and epidural anaesthesia in surgeries on legs
Not Applicable
- Conditions
- Health Condition 1: M80-M85- Disorders of bone density and structure
- Registration Number
- CTRI/2020/02/023181
- Lead Sponsor
- Sangeetha G G
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing elective lower limb surgeries under combined spinal and epidural anaesthesia
American Society of Anaesthesiologist I or II
Exclusion Criteria
Patient refusal
Patients allergic to local anesthetics/Butorphanol/Fentanyl
American Society of Anaesthesiologist III and above
Patients with coagulation disorders
Local site infection
BMI above 30
Poorly controlled Hypertension
Poorly controlled Diabetes mellitus
Patients with cardiac pathology
Pregnant patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the quality and duration of analgesia postoperatively using Visual analogue scale and time of requirement of rescue analgesia respectivelyTimepoint: Postoperative Period
- Secondary Outcome Measures
Name Time Method To assess sedation score and adverse effects such as pruritis, nausea and vomiting, shivering, hemodynamic stability up to 24 hours postoperatively between the two groupsTimepoint: Postoperative Period