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Different doses of Fentanyl with local anaesthetic low dose levobupivacaine for cesarean sectio

Phase 4
Conditions
Health Condition 1: O82- Encounter for cesarean delivery without indication
Registration Number
CTRI/2024/08/072132
Lead Sponsor
Government Medical college, Baroda
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

ASA Grade II patients planned for cesarean section under spinal anaesthesia.

Able to understand study procedure and given consent

Exclusion Criteria

1. Refusal to take part in study

2. Coagulopathy/ Sickle cell disease/ Diabetes Mellitus/ Hypertensive Disorder/ Eclampsia/ Anaemia

3. Allergy or Contraindication to study drugs

4. Any contraindication to spinal anaesthesia

5. Pre-mature rupture of membrane, bleeding P/V, uterine abnormality

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time for complete recovery from Motor block After giving spinal anaesthesiaTimepoint: from zero minute after giving spinal anaesthesia
Secondary Outcome Measures
NameTimeMethod
1. Two segment regression time <br/ ><br>2. Time for Complete recovery from sensory block (Duration of sensory block) <br/ ><br>3. Time to achieve T4-T6 <br/ ><br>4. Duration of analgesia <br/ ><br>5. Patient satisfaction score <br/ ><br>6. Hemodynamic Parameters <br/ ><br>7. Apgar Score in newborn <br/ ><br>8. Any side effects like Nausea, vomiting, hypotension, tachycardia/ bradycardia, respiratory depression, pruritus, high spinal <br/ ><br>Timepoint: Upto 24 hours
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