Comparison of fentanyl and midazolam in spinal anaesthesia in lower segment caesarean section patients
Phase 2
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2023/11/059618
- Lead Sponsor
- Acharya Vinobha Bhave Rural Hospital
- 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 to 35years
2. Patients undergoing cesarean section
3. Primi gravida with gestational age more than 37 weeks
4. Body mass index 20 to 29.9kg/meter square
5. Intact amniotic membrane
6. No history of bleeding tendency or coagulopathies or with any neuromuscular disorders or neurological diseases.
7. No previous uterine operations except cesarean sections
8. Living fetus
9. ASA II
10. Patients giving informed consent.
Exclusion Criteria
1. Patients who are multigravida, previous LSCS.
2. ASA CLASS 3 AND CLASS 4.
3. Patients refusal.
4. Patients with any co-morbities.
5. Patients with infection at the site of injection.
6. Patients with sensitivity to local anaesthetic agent, fentanyl and midazolam.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare and to evaluate efficacy of intrathecal Fentanyl and intrathecal Midazolam added as adjuvant to Bupivacaine 0.5% (heavy) in patients undergoing lower segment caesarean sectionTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Compare the effect of fentanyl & midazolam on <br/ ><br>intraoperative haemodynamics <br/ ><br>The Onset & Duration of Sensory And Motor Block <br/ ><br>To compare the role of fentanyl and midazolam as an adjuvant <br/ ><br>for prevention of side effects <br/ ><br>To access APGAR score <br/ ><br>Timepoint: 24 HOURS