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A clinical trial to study the comparison of two doses of opoid with local anesthetic on characteristics of spinal block in lower abdominal surgeries.

"Comparison of two doses of fentanyl on characteristics of bupivacaine subarachnoid block in infraumbilical surgeries - A randomized prospective double blind study".

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/09/021172
Enrollment
126
Registered
2019-09-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: N218- Other lower urinary tract calculus

Interventions

Intervention1: Fentanyl 20µg characteristics of bupivacaine subarachnoid block: fentanyl 20mcg(0.4ml) is added to 3ml of 0.5% hyperbaric bupivacaine and the solution is made to 3.8ml by adding normal

Sponsors

Department Of Anaesthesiology And Critical Care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients belonging to American Society of Anaesthesiologists physical status grade I & II Age between 18 and 60 years Patients of either sex Patients posted for elective infra-umbilical surgeries under spinal anaesthesia

Exclusion criteria

Exclusion criteria: Coagulation disorders Local site infections Neurological disorders Psychiatric disorders History of spinal surgeries Hypersensitivity to drugs used in the study Pregnant and lactating mothers Those who are not willing to participate in the study

Design outcomes

Primary

MeasureTime frame
Heart rate,systolic blood pressure, diastolic blood pressure and mean arterial pressure, respiratory rate and ramsay sedation score, adverse effects are measured at different pointsTimepoint: Haemodynamic parameters and respiratory rate (RR) will be assessed at 2min, 3min, 6min, 10min, 15min, 30min, 45min, 60min, 2hr, 3hr, 6hr after injection of study drug.

Secondary

MeasureTime frame
number of episodes of hypotension,bradycardia, nausea and vomiting, respiratory depression, pruritusTimepoint: in the intraoperative period during the study period

Countries

India

Contacts

Public ContactDr Valaji Joshna

Sri Venkateswara Institute Of Medical Sciences

drmhraosvims1957@gmail.com9493547651

Outcome results

None listed

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