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A comparative study of ropivacaine with fentanyl in spinal regional anaesthesia in elective lower segment caesarean section surgeries.

A comparative of intrathecal isobaric ropivacaine 0.5 percent with fentanyl versus isobaric ropivacaine 0.5 percent in elective lower segment caesarean section surgeries. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071076
Enrollment
140
Registered
2024-07-23
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: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium

Interventions

Intervention1: SUBARCHNOID BLOCK: INTRATHECAL DRUG ADMISNTRATION Control Intervention1: Isobaric Ropivacaine + Fentanyl: Group RF Injection Ropivacaine 0.5% + Injection Fentanyl 25mcg (0.5ml) total vo

Sponsors

Mahatma Gandhi Medical College and Hospita
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) ASA physical status I-II 2) Pregnant females scheduled for elective lower segment C section surgeries

Exclusion criteria

Exclusion criteria: 1)Patient with known psychiatric disorders, 2)Coagulopathy disorders 3)Infection at the site of block placement 4)Morbid obesity 5)Known Drug Allergie

Design outcomes

Primary

MeasureTime frame
A comparassion intrathecal isobaric ropivacaine 0.5% with fentanyl v/s isobaric ropivacaine 0.5% in elective lower segment caesarean section surgeries to study duration of analgesia,Timepoint: at baseline ,at the time od induction of anaesthesia, after 1minutes of induction, 5minutes, 10minutes, 20 minutes, 30 minutes, 60minutes, 90 minutes, 120 minutes—

Secondary

MeasureTime frame
Time of onset, time to achieve maximum level and duration of sensory block. Time of onset and duration of motor block.Postoperative pain assessment (VAS score) and total analgesic requirement in the first 24 hours in two groups. To assess the side effects like nausea, vomiting, pruritis etc. Timepoint: post-operatively 15 min, 1hr and 2 hr. Time of onset sensory and motor 2 Segment regression sensory and motor.—

Countries

India

Contacts

Public ContactAyush Satishkumar Gupta

Mahatma Gandhi Medical College and Hospital, Jaipur

Silayachisha@gmail.com8107324518

Outcome results

None listed

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