Skip to content

Study comparing the effect of Fentanyl and Dexmedetomidine with Ropivicaine 0.75% Heavy in Spinal Anaesthesia for Lower Abdominal Surgeries

Comparative study of Analgesic Efficacy of Fentantyl and Dexmedetomidine as adjuvant to Intrathecal Hyperbaric Ropivicaine 0.75% for Lower Abdominal Surgeries - A Prospective Double Blinded Randomised Controlled Study - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061181
Enrollment
96
Registered
2024-01-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: R00-R99- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified

Interventions

Intervention1: Ropivicaine with fentanyl: Ropivacaine 0.75% Heavy 3ml with Fentanyl 25mcg. Total volume 3.5ml. Route Intrathecal Frequency- single shot spinal anaesthesia Duration 24 hours post opera

Sponsors

Rajarajeswari medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA I and II patients of either sex. 2.Patients aged between 18 to 60 years 3.Patient height 0f 150cm to 170 cm 4.Patient undergoing elective lower abdominal surgeries

Exclusion criteria

Exclusion criteria: 1.patient refusal 2.allergy to any of the study drugs 3.any contraindications for spinal anaesthesia 4.obesity with weight more than 100 kgs 5.height more than 170cms or less than 150 cms 6.mentally retarded patients 7.pregnant and lactating women 8.abnormalities of spine

Design outcomes

Primary

MeasureTime frame
1.To assess the duration of analgesia defined as the time from intrathecal administration of study drug to first request for rescue analgesia. 2.To assess the duration of motor blockade, defined as the time from onset of motor blockade to complete motor recovery when Bromage scale will be “0 ? Timepoint: 24 hours post operation

Secondary

MeasureTime frame
1.Cumulative analgesic consumption in 24 hours. 2.Maximum VAS pain score. 3.Incidence of hypotension, bradycardia, respiratory depression Timepoint: 24 hours post operation

Countries

India

Contacts

Public ContactDr Ashwini H

Rajarajeshwari medical college and hospital

rishi1126@yahoo.co.in9901292059

Outcome results

None listed

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