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A comparison of regression of sensory block between Nalbuphine and Fentanyl as adjuvant to spinal anaesthesia in hip surgery

A comparison between Nalbuphine and Fentanyl as adjuvant to spinal anaesthesia with hyperbaric Bupivacaine in patients undergoing hip surgery a comparative clinical study. - NIL

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106400
Enrollment
120
Registered
2026-03-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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 Health Condition 2: S720- Fracture of head and neck of femur

Interventions

Intervention1: 0.5% bupivacaine: 0.3mg/kg intrathecal during spinal anaesthesia single shot for intraoperative and postoperative period Intervention2: fentanyl: 25mcg intrathecal during spinal anaesth

Sponsors

Aman Sikdar Department of Anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA Grade I and II

Exclusion criteria

Exclusion criteria: 1.Patient refusal for either the spinal anaesthesia or participation in the study. 2.Any hypersensitivity or contraindication to study drugs. 3.Pregnant or lactating mothers. 4. Hepatic , renal , or cardiopulmonary abnormality. 5.Chronic alcoholism, uncontrolled hypertension, uncontrolled diabetes, long-term drug therapy. 6.Bleeding diathesis, local skin site infections. 7.History of significant neurological, psychiatric, or neuromuscular disorders 8.Patients who have undergone any other clinical trial within the last 3 months

Design outcomes

Primary

MeasureTime frame
To compare the regression time of sensory block to L2 dermatome between two groupsTimepoint: intraoperative to 6 hours post operative

Secondary

MeasureTime frame
To compare the time taken to reach highest level of sensory block among two groupTimepoint: from giving spinal anaesthesia upto 10 min intraoperative;To compare the analgesic duration between two groupsTimepoint: intraoperative & 6 hours postoperative;To compare the side effects between two groups.Timepoint: intraoperative & 6 hours postoperative

Countries

India

Contacts

Public ContactDr. Anjan Das

College of Medicine and Sagore Dutta Hospital

anjan2k8@yahoo.com9874171440

Outcome results

None listed

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