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Effect of region specific anesthesia in forearm and hand surgery using latest ultrasound technique.

Comparison of ultrasound guided costoclavicular brachial plexus block versus supraclavicular brachial plexus block for forearm and hand surgery: A randomized clinical trial. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/041029
Enrollment
64
Registered
2022-03-11
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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: M848- Other disorders of continuity of bone

Interventions

Intervention1: Supraclavicular brachialplexus block: Ultrasound guided Supraclavicular brachial plexus block with 20 ml of 0.5% ropivacaine once in the preoperative area . Intervention2: costoclavicul

Sponsors

Dr Laxman Kumar Senapati
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 18-75 years with American Society of Anesthesiologists physical status (ASA) I-III scheduled to undergo surgery of the elbow, forearm, wrist or hand under brachial plexus block (BPB).

Exclusion criteria

Exclusion criteria: 1. Patient refusal to participate 2. Contraindication to peripheral nerve blocks 3. Patients with pre-existing neuropathy 4. Prior surgery of the infraclavicular fossa 5. Pregnancy and body mass index more than 30 kg/m2

Design outcomes

Primary

MeasureTime frame
Sensory and motor blockade score as per 3-point scale. (Sensorimotor blockade score as per 3-point scale- at least 14 out of 16)Timepoint: Sensory and motor blockade score as per 3-point scale every 3 minute untill 30 minute after injection of drug like 3 min, 6 min, 9 min, 12 min, 15 min, 18 min, 21 min, 24 min, 27 min and 30 min after block.

Secondary

MeasureTime frame
-Block performance time -Sensory block duration -Motor block duration -Post-operative VAS score to know duration of analgesia -Time to first rescue analgesia requirement - Patient satisfaction -occurrence of side effects Timepoint: up to 24 hour in the postoperative period.

Countries

India

Contacts

Public ContactDr Laxman Kumar Senapati

Kalinga Institute Of Medical Sciences

meet.laxmans1@gmail.com7325919472

Outcome results

None listed

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