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A Study Comparing Supraclavicular and Infraclavicular Blocks for Arm and Forearm Operations

A comparison of ultrasound guided supraclavicular block versus infraclavicular block for elbow and below elbow surgeries - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112184
Enrollment
68
Registered
2026-06-08
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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: supraclavicular block: Group S- Will receive ultrasound guided supraclavicular block with 25ml of 0.5% Bupivacaine + 2ml (8mg) Dexamethasone and the effects monitored for the next 2hrs

Sponsors

Shri Ram Murti Smarak Institue Of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 1, 2 and 3 patients undergoing elective elbow and below elbow surgeries body Mass index less than 35

Exclusion criteria

Exclusion criteria: ASA grade 4 unwillingness to be a part of trial patients with known hypersensitivity to local anaesthetics patient with infection at the site of injection patient with bleeding disorders or those on anti-coagulants

Design outcomes

Primary

MeasureTime frame
To compare the quality of block among the groupsTimepoint: Baseline After Block 5 mins 15 mins 30 mins 45 mins 60 mins 75 mins 90 mins 105 mins 120 mins

Secondary

MeasureTime frame
To compare the time of onset of sensory block among the groups.Timepoint: Baseline After Block 5 mins 15 mins 30 mins 45 mins 60 mins 75 mins 90 mins 105 mins 120 mins;To compare the time of onset of motor block among the groups.Timepoint: Baseline After Block 5 mins 15 mins 30 mins 45 mins 60 mins 75 mins 90 mins 105 mins 120 mins;To compare the block performance time among the groupsTimepoint: Baseline After Block 5 mins 15 mins 30 mins 45 mins 60 mins 75 mins 90 mins 105 mins 120 mins;To compare the total analgesic consumption 24 hours, post operatively among the groups.Timepoint: Baseline After Block 5 mins 15 mins 30 mins 45 mins 60 mins 75 mins 90 mins 105 mins 120 mins;To compare the incidence of adverse events or complications among both the groupsTimepoint: Baseline After Block 5 mins 15 mins 30 mins 45 mins 60 mins 75 mins 90 mins 105 mins 120 mins

Countries

India

Contacts

Public ContactDr Shailesh Kumar Lohani

SRMS IMS bareilly

juhibdsaran@gmail.com7088973697

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026