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Clinical Trials/IRCT20180627040258N1
IRCT20180627040258N1
Recruiting
Phase 2

A clinical trial to compare the effectiveness of ketamine, propofol/ketamin with propofol/fentanilel for procedure sedation and analgesia of reduction of shoulder dislocation.

Artesh University of Medical Sciences0 sites150 target enrollmentTBD
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Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Artesh University of Medical Sciences
Enrollment
150
Status
Recruiting
Last Updated
7 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Artesh University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • •Aged between 15 and 40 years
  • •Lake of underlying disease such as blood pressure, diabetic, cardiovascular disease, and etc
  • •Having dislocation orthopedic removable at emergency
  • •Normal examination of the neuromuscular system
  • •Non allergenic to sedative drug

Exclusion Criteria

  • •Cardiovascular instability
  • •Having low saccharification
  • •Having multiple trauma
  • •Possibility of the abdomen or chest bleeding
  • •Having head trauma
  • •Decreased alertness

Outcomes

Primary Outcomes

Not specified

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