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Study to compare effects of drug named nalbuphine and buprenorphine when used together with drug bupivacaine in blocking brachial plexus nerve bundle through above clavicle bone approach using ultrasound technique.

A COMPARATIVE STUDY TO EVALUATE THE EFFICACY OF NALBUPHINE VERSUS BUPRENORPHINE AS AN ADJUVANT TO 0.5% BUPIVACAINE IN ULTRASOUND GUIDED SUPRACLAVICULAR BRACHIAL PLEXUS BLOCK IN UPPER LIMB SURGERIES

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/049107
Enrollment
50
Registered
2023-01-19
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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: V232- Unspecified motorcycle rider injured in collision with car, pick-up truck or van in nontraffic accident

Interventions

Intervention1: Inj Nalbuphine: 10mg along with 19ml 0.5% Bupivacaine for supraclavicular brachial plexus block Control Intervention1: Inj Buprenorphine: 150micrograms with 19ml Bupivacaine and 0.5ml N

Sponsors

Dr Malathi
Lead Sponsor
Dr Kantharaja H E
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients providing written informed consent voluntarily. 2) Patients belonging to age group 18 - 60 years of both sexes. 3) Patients measuring height 150-180cms and weighing 50-80kgs. 4) Patients scheduled for upper limb orthopedic surgery under supraclavicular brachial plexus block. 5) American society of anaesthesiologists (ASA) Grade I and II

Exclusion criteria

Exclusion criteria: 1) Patients refusing written informed consent. 2) Patients having infections at the site of injection. 3) Clinically significant coagulopathy. 4) Allergic to the study drugs. 5) Cardiogenic or hypovolemic shock. 6) Preexisting motor and sensory deficit. 7) Respiratory insufficiency.

Design outcomes

Primary

MeasureTime frame
1) Onset of sensory block 2) Onset of motor block 3) Duration of sensory block 4) Duration of motor block 5) Duration of postoperative analgesiaTimepoint: 24 hours

Secondary

MeasureTime frame
1)Heart Rate 2)Systolic BP 3)Diastolic BP 4)Mean BP 5)respiratory rate 6)saturation 7)Sedation score 8)VAS score 9)ComplicationsTimepoint: 24 hours

Countries

India

Contacts

Public ContactDr Kantharaja H E

Bangalore Medical College and Research Institute, Bangalore

kanthu.hirenallur@gmail.com9739006556

Outcome results

None listed

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