Status:
COMPLETED
Procedural Sedation Using Propofol Versus Midazolam/Ketamine in the Adult Emergency Department
Lead Sponsor:
Tel-Aviv Sourasky Medical Center
Conditions:
Procedural Sedation
Eligibility:
All Genders
18-65 years
Phase:
PHASE4
Brief Summary
The use of procedural sedation and analgesia (PSA) to accomplish painful procedures in the emergency department (ED) has become a standard of practice over the last decade. Substantial variance exists...
Eligibility Criteria
Inclusion
- Patients with orthopedic injuries requiring painful manipulation (i.e. reduction of fracture or dislocation, drainage of abscess, suture of extensive laceration)
- Age between18-65 years
- American Society of Anesthesiologists (ASA) score of 1 or 2
- Systolic blood pressure higher than 90 mmHg and lower than 160 mmHg before initiating sedation
- Willingness and ability to provide an informed consent
- No known hypersensitivity to either medication
- No evidence of intoxication
- No recent heavy meal.
Exclusion
- Pregnant women and patients who do not meet the above criteria will be excluded.
Key Trial Info
Start Date :
November 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2009
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT00784498
Start Date
November 1 2008
End Date
September 1 2009
Last Update
August 3 2010
Active Locations (1)
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1
Tel Aviv Sourasky Medical Center
Tel Aviv, Israel