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To reduce pain in fracture patients by giving local nerve block vs intravenous opiod

To study the utility of ultrasound guided block for analgesia in patients of acute limb injuries presenting to emergency department: a randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061719
Enrollment
84
Registered
2024-01-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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: Site specific nerve block: Ultrasound guided site specific nerve block according to location of fracture. Nerve block is performed by inserting a nerve block needle under ultrasound gui

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult of both gender from eighteen to eighty years presenting to emergency department with history of trauma and triaged as yellow or green and having upper or lower limb fractures with on arrival pain score greater than or equal to seven and patient or legally authorized representative gives consent

Exclusion criteria

Exclusion criteria: Patient or legally authorized representative is unable or unwilling to give consent or red triaged patients or patients with unstable vitals on arrival or less than eighteen years or greater than eighty years or patients with life threatening comorbidities or history of hypersensitivity or known contraindication to local anaesthetics or pain score less than seven

Design outcomes

Primary

MeasureTime frame
To study and compare the pain score reduction during initial six hours of interventionTimepoint: 1hour,3hour,6hour

Secondary

MeasureTime frame
To study complications of block procedure & compare with complications of opiod usageTimepoint: Over 6 hours;To study the length of emergency department stayTimepoint: In hours;To study the reduction in opiod usage due to block procedureTimepoint: Over 6 hours;To study the time taken to do the procedureTimepoint: In minutes;To study the time taken to reduce the pain after interventionTimepoint: In minutes

Countries

India

Contacts

Public ContactDr Barada Prasad Debasish Panda

All India Institute of Medical Sciences, New Delhi

drsinha123@gmail.com8518881749

Outcome results

None listed

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