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Comparing three different approaches of a nerve block for patients undergoing humerus surgeries to assess the better technique for pain management.

A study between three different ultrasound-guided techniques of Intercostobrachial nerve block - distal approach versus proximal approach versus supra-axillary approach in proximal humerus surgeries: A randomised three arm concurrent parallel clinical trial. - nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092495
Enrollment
120
Registered
2025-08-06
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: intercostobrachial nerve block (distal approach): 3 mL of 0.25% ropivacaine + 3 mL of 2% lignocaine with adrenaline Intervention2: intercostobrachial nerve block (distal approach): 3 mL

Sponsors

Dr.Thamizh Thendral. A
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and 2 BMI less than 30

Exclusion criteria

Exclusion criteria: Patients unwilling to enroll for the study Change in the plan of anaesthesia. Patients with a history of allergy to the drugs used in the study Patients with infection at the site of injection. Duration of surgeries extending beyond 3hrs. Neuropathy

Design outcomes

Primary

MeasureTime frame
To compare the analgesic efficacy in terms of onset of sensory blockade of ultrasound guided Intercostobrachial Nerve Block by three different approaches - distal approach versus proximal approach versus supra-axillary approach for patients undergoing proximal humerus surgeries done via delto-pectoral approach.Timepoint: The Sensory block onset will be assessed every 2 minutes for 15 minutes via pinprick testing over the anteromedial and posteromedial upper arm.

Secondary

MeasureTime frame
To assess the ease of technique in terms of duration of procedureTimepoint: Duration of the procedure will be recorded combining Landmark identification time (USG localization of target area) and Block execution time (from needle insertion to withdrawal after injecting the drug).;To assess the incidence of ICBN block failures.Timepoint: No sensory loss after 15 min after giving block will be noted;To assess analgesic efficacy post operatively using Visual analogue scale score.Timepoint: post operatively at at 0,2,4,6,12, and 24 hours;To assess incidence of complications like hematoma, nerve injury and pneumothorax.Timepoint: while administering the nerve block

Countries

India

Contacts

Public ContactThamizh Thendral

Aarupadaiveedu Medical college and research institute

thendral4991@gmail.com9789898804

Outcome results

None listed

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