A comparison of sedation with thiopental–fentanyl versus propofol–fentanyl for anterior shoulder dislocation reduction in Emergency department

Phase 2

• Conditions: Anterior Shoulder Dislocations.; Anterior dislocation of unspecified humerus, initial encounter; S43.016A

• Registration Number: IRCT20210626051714N1
• Lead Sponsor: Zanjan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 August 2021

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Willingness to participate in the study
People 18 to 40 years old with anterior shoulder dislocation

Exclusion Criteria

Patients with fractures and major dislocations
Other major injuries with hemodynamic disturbances
History of substance abuse
Patients with allergies to any of the drugs
Pregnancy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of sedation in three stages 1- Start of sedation 2- Between sedation and awakening 3- Between awakening to full consciousness. Timepoint: 1- Start of sedation 2- Between sedation and awakening 3- Between awakening to full consciousness. Method of measurement: Using a stopwatch.