Comparison of postoperative pain relief by using fentanyl given as transdermal patch and epidural infusio
Not Applicable
- Conditions
- Health Condition 1: C55- Malignant neoplasm of uterus, partunspecified
- Registration Number
- CTRI/2021/05/033653
- Lead Sponsor
- Dept Of Anaesthesiology and Critical Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Age between 18-60 years
2. ASA I-II
3. Body mass index 20 - 35kg/m2
4. Laparotomy with below umbilicus incision.
Exclusion Criteria
1. Known allergy to the study drug
2. Contraindication to neuraxial blockade
3. Patients with cognitive impairment
4. Uncontrolled cardiovascular / hepatic / renal disease or impaired pulmonary function.
5. Patients having intolerance to opioid
6. Pregnant and breastfeeding females
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the post-operative pain scores in patients receiving transdermal and epidural fentanylTimepoint: 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method To compare the adverse events in patients receiving transdermal and epidural fentanylTimepoint: 24 hours postoperatively