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Nerve block with dexmedetomidine for paediatric hand surgery

A comparative study to evaluate analgesic efficacy of ultrasound guided forearm nerve block with dexmedetomidine as adjuvant for hand surgery in paediatric patients: A randomized trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055547
Enrollment
75
Registered
2023-07-24
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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: Forearm nerve block with 0.25% ropivacaine with 0.5mcg/kg dexmedetomidine.: children undergoing hand surgery will recieve forearm nerve block with 0.25% ropivacaine with 0.5mcg/kg dex

Sponsors

ALL INDIA INSTITUTE OF MEDICAL SCIENCES
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Children between age group 1-12 years 2. Either sex 3. ASA I & II 4. Elective cases for hand surgery. 5. Consent given

Exclusion criteria

Exclusion criteria: 1.Parents refusal to participate in the study 2.Patient undergoing emergency surgery. 3.Children with significant cardiovascular, neurological, pulmonary, or genetic disorders. 4.Known allergy to local anaesthetic agent.

Design outcomes

Primary

MeasureTime frame
To compare analgesic efficacy of forearm nerve block with ropivcaine alone or ropivacaine combined with different doses of dexmedetomidine as adjuvant for post-operative pain using pain score and total fentanyl requirement post-surgery for 12 hours.Timepoint: Patient will be monitored from the point of nerve block upto 12 hours post operatively for the study.

Secondary

MeasureTime frame
1.Intraoperative hemodynamic variables like HR, BP, sp02.Timepoint: Patient will be monitored from the point of nerve block upto end of surgery.;2.Duration of analgesia - Time to first dose of analgesicTimepoint: Time from end of surgery to requirement of first rescue analgesia in post operative period;3.Total analgesic consumption in peri-operative period.Timepoint: Total analgesic consumption from start of surgery to 12 hours postoperatively;4.Comparing the post operative pain by FLACC score (1-7years)/ NRS score(7-12 years) at immediate postoperative period, 1 hour, 2 hours , 4 hours, 6 hours and 12 hours post-surgeryTimepoint: Immediate postoperative period, 1 hour, 2 hours , 4 hours, 6 hours and 12 hours post-surgery;5. Parental satisfaction score at end of 4 hrs and 12 hours post-surgery (5-point Likert scale)Timepoint: At end of 4 hrs and 12 hours post-surgery;6.Incidence of side effects like sedation, hypotension, bradycardiaTimepoint: Time from end of surgery to 12 hours post operatively

Countries

India

Contacts

Public ContactHEENA GARG

AIIMS NEW DELHI

gargheena11@gmail.com9464533877

Outcome results

None listed

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