A clinical trial to study the effect of two drugs, Fentanyl and Buprenorphine as an adjuvant to Bupivacaine in spinal anaesthesia for Lower Segment Cesarean Sectio
Phase 3
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2021/07/034806
- Lead Sponsor
- Bharati Vidyapeeth Deemed to be University medical college and research center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA II
Exclusion Criteria
�ASA III/IV/V
�Patients with comorbidites during pregnancy- gestational diabetes mellitus, pregnancy induce hypertension, heart disease
�Contraindications of spinal anaesthesia- raised intracranial pressure, local infection, coagulation disorders
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method �post Operative regain of sensory block and motor block <br/ ><br>�post operative duration of first rescue analgesia demandTimepoint: Observation of motor and sensory block after spinal anaesthesia in lower segment caesarean section every 5 minutes upto 10 minutes then every 10 minutes upto end of surgery
- Secondary Outcome Measures
Name Time Method Hemodynamic stability after giving spinal anaesthesia in lower segment caesarean sectionTimepoint: Heart rate, systolic blood pressure, diastolic blood pressure, respiratory rate, oxygen saturation for every 5 min for 10 minutes then every 10 minutes upto end of surgery