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Comparing effects of morphine and ketamine on pain relief

Phase 3
Recruiting
Conditions
Pain.
Other soft tissue disorders, not elsewhere classified
Registration Number
IRCT2017041221480N6
Lead Sponsor
Vice chancellor for research, Mazandaran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
156
Inclusion Criteria

Fracture of long bones in upper or lower extremities caused by blunt and direct trauma referring to the emergency ward; needing inject-able sedative
Exclusion criteria: History of psychiatric, liver and kidney diseases, stroke, asthma and other cardiac and respiratory diseases; weight of below 45 or above 155 kg; pregnant or breastfeeding women; pressure of above 18 or below 90 mm Hg; heart rate of below 50 or above 150 per minute; respiration rate of below 10 or above 30 per minute; reduced consciousness; blow to the head or eyes; multiple trauma; allergy to the sedatives used in the research; drug addiction; use of inject-able drugs; fracture in the parts other than long bones; fracture with dislocation or fracture with extreme displacement that requires a reduction ; open fracture; compartment syndrome; lack of tendency to participate in the project; receiving sedatives before the research

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Start the intervention, in minutes (30, 60, 90, 120, 180, 240) after the intervention. Method of measurement: Visual scale of pain.
Secondary Outcome Measures
NameTimeMethod
Blood Pressure. Timepoint: 0,30,60,120,180,240 minutes after intervention. Method of measurement: MmHg With manometer.;Respiratory rate. Timepoint: 0,30,60,120,180,240 minutes after intervention. Method of measurement: Count the respiration rate.
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