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Comparison of tourniquet pain between two types of brachial plexus block

Evaluation of tourniquet pain with ultrasound guided infraclavicular and axillary approach of brachial plexus block in adult patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050667
Enrollment
40
Registered
2023-03-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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: Brachial plexus block: Axillary or infraclavicular approach of brachial plexus block will be used Intervention2: Ultrasound guided brachial plexus block: infraclavicular block will be a

Sponsors

Department of Anesthesia, Pt BD Sharma PGIMS, Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I to III, scheduled to undergo orthopaedic or plastic surgery distal to elbow with anticipated tourniquet duration greater than 45 minutes will be included

Exclusion criteria

Exclusion criteria: Patients with Contraindications to regional Anesthesia, local infection , distortion of local anatomy, allergy to local anaesthetics, chronic pain syndrome, clinically significant cognitive impairment, axillary clearance in past, pregnancy, history of peripheral neuropathy, refusal to give consent will be excluded.

Design outcomes

Primary

MeasureTime frame
Severity and incidence of tourniquet pain in both groupsTimepoint: Every 30 minutes during the intraoperative period

Secondary

MeasureTime frame
Block performance time, block onset time, number of failed blocks, patient satisfaction and adverse effects will be compared between the two approachesTimepoint: every 5 minutes after application of block till 30 minutes

Countries

India

Contacts

Public ContactKarishma Dhankhar

Department of Anaesthesia, Pandit BD Sharma PGIMS Rohtak

drbmamta@gmail.com9812789476

Outcome results

None listed

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