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Fentanyl prolonged analgesia when added to heavy Ropivacaine in caesarean section under spinal anaesthesia.

Comparison of the effect of hyperbaric Ropivacaine with or without fentanyl in parturient undergoing elective caesarean section under subarachnoid block.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/09/045898
Enrollment
50
Registered
2022-09-26
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Spinal anaesthesia: Comparative drugs hyperbaric Ropivacaine with fentanyl or hyperbaric Ropivacaine with normal saline will be given in subarachnoid block and the effect of post operat

Sponsors

Dr SN medical college Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All pregnant female of age between 20 ââ?¬â?? 35 years with more than 37 weeks of singleton pregnancy of ASA physical status of grade ââ?¬â?? II only undergoing elective LSCS under spinal anesthesia will be included

Exclusion criteria

Exclusion criteria: 1.Patients refusing for being part of the study 2.Patients who had obstetric complications, multiple gestation or suspected fetal abnormality. 3.History of spine deformity or spine surgery, hepatic failure, neuromuscular disorders. 4.Chronic history of headache and backache, infection in the back. 5.Any absolute or relative contraindication to study drug. 6.Uncooperative patients. 7.Coagulopathy or patients taking anticoagulants 8.Patient with history of cardiac or respiratory diseases

Design outcomes

Primary

MeasureTime frame
To compare the duration of analgesia in the early postoperative period with or without fentanyl added in hyperbaric ropivacaine in parturient undergoing cesarean section under spinal anaesthesia.Timepoint: 24 hours

Secondary

MeasureTime frame
The following parameters will be compared in both the group 1. Comparison of time to onset of sensory block 2. Comparison of time to peak sensory block 3. Comparison of the highest dermatomal level of block achieved 4. Comparison of total duration of sensory block 5. Comparison of the time to onset of motor block 6. Comparison of total duration of motor block 7. The intraoperative hemodynamic changes 8. Adverse events or complication 9. Patient satisfaction Timepoint: 24 hours

Countries

India

Contacts

Public ContactDr Neelam Meena

Dr SN Medical College

drneelamsiddhimeena@gmail.com8302537601

Outcome results

None listed

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