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Propofol versus Midazolam for Procedural Sedation of Anterior Shoulder Dislocatio

Not Applicable
Conditions
Dislocation of shoulder joint.
Contusion of shoulder and upper arm
Registration Number
IRCT201501236238N2
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
48
Inclusion Criteria

The inclusion criteria include anterior dislocation of the shoulder and over 18 years of age. The exclusion criteria include hypersensitivity to midazolam, propofol, or fentanyl; other injury (fracture around shoulder or other limb); intake of food or fluid during last 4 hours; presence of airway difficulty; sensory problems; motor problems, vascular problems, and consumption of alcohol or other recreational drug during past 6 hours.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Success of reduction. Timepoint: after each reducing process. Method of measurement: Physical examination and X-ray.
Secondary Outcome Measures
NameTimeMethod
Complication. Timepoint: after reduction and each subsequesnt visit. Method of measurement: History, physical examination and X-ray.
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