Pain control in burn patients

Phase 2

• Conditions: Pain control in burn patients.; Burns of multiple regions, at least one burn of third degree mentioned; T29.3

• Registration Number: IRCT201406116186N5
• Lead Sponsor: Vice chancellor for research of Guilan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 2 May 2022

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 66

Inclusion Criteria

Age between 18-60 years
American society Anesthesiologists class I, II
total body surface area burns 20% to 40%,
second and third-degree burn in upper and lower limbs and trunk

Exclusion Criteria

Sensitivity to the local anesthetics and opiates
pregnancy
a history of neuropathic and chronic pain
addiction
hepato-renal diseases
cardiac disease especially arrhythmia

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: evaluated at baseline and after 1, 2, 4, 8, 12, 16, 20, 24 hours after intervention. Method of measurement: 11-point Numerical Rating Scale (NRS).;Sedation level. Timepoint: evaluated at baseline and after 1, 2, 4, 8, 12, 16, 20, 24 hours after intervention. Method of measurement: Ramsay Score.

Secondary Outcome Measures

Name	Time	Method
Complications. Timepoint: evaluated at baseline and after1, 2, 4, 8, 12, 16, 20, 24 hours after intervention. Method of measurement: observation of any complications such as convulsion, nausea, vomiting, pruritus, urine retention, drowsiness, and respiratory depression.