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A comparative study between epidural nalbuphine and fentanyl for analgesic efficacy in patients undergoing infraumbilical surgeries under spinal anesthesia

A comparative study of epidural nalbuphine versus fentanyl for analgesic efficacy in patients undergoing infraumbilical surgeries under spinal anesthesia. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091587
Enrollment
60
Registered
2025-07-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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: Nalbuphine: Epidural nalbuphine 5mg with 0.125 %bupivacaine diluted to 9ml normal saline Control Intervention1: Nalbuphine , Fentanyl: Epidural nalbuphine 5mg + 0.125% bupivacaine dilu

Sponsors

Dr Varshini G
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients giving consent, ASA grade 1 and 2, BMI 18 to 29 kg/m^2

Exclusion criteria

Exclusion criteria: Allergy to local anesthetic, spine deformity, coagulopathy,chronic pain syndromes, cardiac diseases, liver and kidney dysfunction, neurological disorders, pregnancy and breastfeeding mothers, technical failure, patients on tricyclic antidepressants, alpha 2 agonist and opioids

Design outcomes

Primary

MeasureTime frame
Analgesic efficacy of epidural nalbuphine versus fentanyl in terms of duration of Analgesia in patients undergoing infraumbilical surgeries under spinal anesthesia in 24 hoursTimepoint: Analgesic efficacy of epidural nalbuphine versus fentanyl in terms of duration of Analgesia in patients undergoing infraumbilical surgeries under spinal anesthesia in 24 hours—

Secondary

MeasureTime frame
Compare onset of sensory & motor blockade, duration of motor blockade, 2 segment regression, VAS, ramsay sedation scale, time of first rescue analgesia.Timepoint: In 24 hrs;Assess hemodynamic parameters perioperativelyTimepoint: 24 hours;Assess incidence of any side effects of study drugsTimepoint: In 24 hours—

Countries

India

Contacts

Public ContactDr Nethra SS

Bangalore medical college and research institute

nethra.surhonne@gmail.com9448171403

Outcome results

None listed

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