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A Randomised controlled trial of infraclavicular versus costoclavicular approach of Infraclavicular block in upper limb surgery

Randomised controlled trial to assess the postoperative analgesic efficacy of continuous paracoracoid versus costoclavicular approach to infraclavicular block in upper limb surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035491
Enrollment
100
Registered
2021-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M849- Disorder of continuity of bone, unspecified

Interventions

Intervention1: Group1 infraclavicular block (Paracoracoid approach): Group 1 (Paracoracoid approach) Transducer will be positioned medially to the coracoid process below clavicle in parasagittal axis

Sponsors

Lady hardinge medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients >18yrs of ASA1 and 2 of either sex.

Exclusion criteria

Exclusion criteria: 1.Upper limb surgeries above mid humerus level. 2. Any known drug allergies. 3.Contraindication to nerve block like coagulopathy, bleeding diathesis and local infections. 4.Preexisting neurological deficit.

Design outcomes

Primary

MeasureTime frame
Mean opioid consumption(mg/kg) at the end of 24 hours poatoperatively in both paracoracoid and costoclavicular infraclavicular block groups.Timepoint: Mean opioid consumption(mg/kg) at the end of 24 hours poatoperatively in both paracoracoid and costoclavicular infraclavicular block groups.

Secondary

MeasureTime frame
1. To compare the Pain score (Numerical Rating Scale (NRS)) on rest at 0,6,12 and24 hours postoperatively in both groups. 2. To compare the Pain score (NRS) on limb movement at 0,6,12 and 24 hours postoperatively in both groups. 3. To assess any catheter related complications (catheter dislodgement, erythema, hematoma at the site of catheter insertion) in both groups.Timepoint: 0,6,12 and 24 hours postoperatively

Countries

India

Contacts

Public ContactNitin hayaran

Lady Hardinge Medical College

nhayaran97@gmail.com011-23408259

Outcome results

None listed

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