To study the success rate of a new type of upper limb block in children using ultrasound

Ultrasound guided costoclavicular block in paediatric population : A prospective observational study.

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/03/024234

Enrollment

Registered

2020-03-25

Start date

Unknown

Completion date

Unknown

Last updated

2023-05-29

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

Conditions

Health Condition 1: Q709- Syndactyly, unspecified

Interventions

Intervention1: costoclavicular block: Ropivocaine 0.5% at the dose of 0.5mL/kg will be utilised for ultrasound guided costoclavicular block Control Intervention1: Not applicable: Single arm study

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age 2-12 years 2. Patients scheduled for elective upper limb surgery (below elbow) 3. ASA Status I or II

Exclusion criteria

Exclusion criteria: 1. Refusal by Parents 2. Known allergy to local anaesthetics 3. Local site infection 4. Bleeding diathesis

Design outcomes

Primary

Measure	Time frame
Success rate of costoclavicular block in paediatric patients Timepoint: 15 minutes after giving block	—

Secondary

Measure	Time frame
Assess the ease of needlingTimepoint: Time-0 (while giving block);Describe the relationship of 3 cords of brachial plexus to axillary arteryTimepoint: time -0 (while giving block);Incidence of vascular puncture, pleural punctureTimepoint: Time-0( while giving block);Pain scoreTimepoint: 10 min, 30 min, 2,4,6 and 8 hours	—

Countries

India

Contacts

Public ContactDr Ashwin M

All India Institute of Medical Sciences New Delhi

kanil.aiims@gmail.com8800314575

Outcome results

None listed

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