Intravenous fentanyl vs. erector spinae block in chest trauma pai

Phase 3

• Conditions: unspecified injury of thorax; S29.9XXA; nspecified injury of thorax (chest trauma).

• Registration Number: IRCT20131226015941N7
• Lead Sponsor: Kerman University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 May 2019

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Patients over 16 years of age presenting to the emergency department with chest trauma
initial pain score over 5 (from 10)

Exclusion Criteria

presence of distracting injuries
impaired consciousness
hypersensitivity to lidocaine or fentanyl
presence of coagulopathy
presence of any sensory impairment like peripheral neuropathy
receiving pain killers before enrollment
those who are not willing to participate or to continue their cooperation
need for surgical intervention through the chest wall (including tube thoracostomy)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score. Timepoint: 20 minutes and 1 hour after injection or block. Method of measurement: asking the patient by numeric rating scale.

Secondary Outcome Measures

Name	Time	Method
Total dose of intravenous fentanyl administered to achieve adequate analgesia. Timepoint: The first 6 hours of admission in the emergency department. Method of measurement: recording by the investigator.;Adverse reactions of the intervention(s). Timepoint: at the discharge time. Method of measurement: assessment by the investigator.