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

Efficacy of Different Doses of Fentanyl With Intrathecal Low Dose Levobupivacaine on Recovery profile in cesarean section A Prospective Randomized Double Blind Study - NILL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072132
Enrollment
285
Registered
2024-08-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O82- Encounter for cesarean delivery without indication

Interventions

Intervention1: Fentanyl 10 microgram with levobupivacaine: After preanesthetic evaluation patients meeting inclusion criteria will be selected. Operation theatre with all necessary equipments and drug

Sponsors

Government Medical college, Baroda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA Grade II patients planned for cesarean section under spinal anaesthesia. Able to understand study procedure and given consent

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Time for complete recovery from Motor block After giving spinal anaesthesiaTimepoint: from zero minute after giving spinal anaesthesia

Secondary

MeasureTime frame
1. Two segment regression time 2. Time for Complete recovery from sensory block (Duration of sensory block) 3. Time to achieve T4-T6 4. Duration of analgesia 5. Patient satisfaction score 6. Hemodynamic Parameters 7. Apgar Score in newborn 8. Any side effects like Nausea, vomiting, hypotension, tachycardia/ bradycardia, respiratory depression, pruritus, high spinal Timepoint: Upto 24 hours

Countries

India

Contacts

Public ContactDr Hemangini Patel

Government medical college, Baroda

afroza7887@gmail.com9825359856

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026