Comparison of labor epidural with three different doses of fentanyl
Phase 3
Completed
- Registration Number
- CTRI/2020/07/026662
- Lead Sponsor
- Amrita Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All consenting parturients of the American society of anaesthesiologists, grade1 and 2 having uncomplicated cephalic singleton pregnancy and desirous of having a labour epidural
Exclusion Criteria
Hypersensitivity to study drugs, bleeding disorders, decreased platelet counts, sepsis, spinal column deformities, history of spine surgery and if parturient delivers before administering the second bolus dose.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of duration of adequate analgesia with each bolusTimepoint: Till delivery of baby
- Secondary Outcome Measures
Name Time Method onset of analgesia, incidence of sedation, pruritus, instrumental delivery, conversion to caesarean section and fetal outcomes like bradycardia, fetal acidosis and Apgar.Timepoint: Till delivery of baby