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Effect of intravenous diazepam in reduction shoulder joint dislocatio

Phase 3
Recruiting
Conditions
Shoulder dislocation.
Subluxation and dislocation of shoulder joint
Registration Number
IRCT20170313033051N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

The need for analgesia for joint reduction
No severe underlying diseases
Age 18 to 65 years
The desire to participate in the study

Exclusion Criteria

Lack of desire to participate in the study
Sensitivity to drug used in study
Pregnancy
Hemodynamic instability
Presence of fracture associated with dislocation

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patient satisfaction according to pain scale. Timepoint: Before reduction, during the reduction and after the reduction. Method of measurement: Using Visual Analogue Scale.;Uncomplicated joint reduction. Timepoint: During the reduction and after the reduction with intervals 15 minutes for 2 hours. Method of measurement: Examination of vital signs and level of consciousness during and after the procedure.;Physician Satisfaction. Timepoint: After reduction. Method of measurement: sing Likert scale.
Secondary Outcome Measures
NameTimeMethod
o need for post-reduction care. Timepoint: During and after the reduction for 2 hours and at intervals of 15 minutes. Method of measurement: Using Glasgow Coma Scale and vital sign monitoring with sphygmomanometer and pulse oximeter.
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