CTRI/2023/11/059618
Not yet recruiting
Phase 2
A comparative study to evaluate efficacy of intrathecal fentanyl and intrathecal midazolam added as adjuvant to Bupivacaine 0.5 (heavy) in patients undergoing LSCs - NI
Acharya Vinobha Bhave Rural Hospital0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Acharya Vinobha Bhave Rural Hospital
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
- •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.
Outcomes
Primary Outcomes
Not specified
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