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â??Comparative study of two drugs, Fentanyl vs Clonidine when used with standard drug Bupivacaine, in patients undergoing spinal anaesthesia to find out which has better tolerance and pain relief in lower abdominal procedures .â??

â??Comparative study of Bupivacaine-Fentanyl vs. Bupivacaine-Clonidine in patients undergoing spinal anaesthesia for lower abdominal surgery.â??

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/040869
Enrollment
200
Registered
2022-03-07
Start date
Unknown
Completion date
Unknown
Last updated
2022-04-04

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 with Bupivacaine- Fentanyl: i) Written informed consent to perform subarachnoid block will be taken from all the patients. iii) Grouping and Randomization: 100 patien

Sponsors

Ramakrishna Mission Seva Pratisthan And Vivekananda Institute Of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who gives written consent. b) ASA-I&II c) Age 18-60 years. d) Any patient posted for elective lower abdominal surgery that can be done under subarachnoid block.

Exclusion criteria

Exclusion criteria: Patient who doesnâ??t give consent to participate. b) Any contraindication to SAB. c) Patient requiring intraoperative added any general anaesthetic aid. d) Deaf patient e) Mentally retarded patient/Dementia. f) Patient with psychiatric disorder.

Design outcomes

Primary

MeasureTime frame
Comparison of analgesic duration following, Bupivacaine-Fentanyl vs Bupivacaine-ClonidineTimepoint: Comparison of analgesic duration following, Bupivacaine-Fentanyl vs Bupivacaine-Clonidine

Secondary

MeasureTime frame
Comparison of postoperative pain relief following, Bupivacaine-Fentanyl vs Bupivacaine-ClonidineTimepoint: Continuous ECG in lead II, SBP, DBP, MAP, HR, RR, SpO2 will be recorded 15 minutes before and at the time of spinal anaesthesia, then at 1 minute, at 3 minute, at 5 minute, thereafter at 5 minutes interval through out the entire surgical procedure and at 15 minutes interval during first 60 minutes of post-operative period.

Countries

India

Contacts

Public ContactDr Keya Chakraborty

RKMSP & VIMS Kolkata

drkeyachakraborty21@gmail.com9830183464

Outcome results

None listed

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