Pain control in trauma patients

Not Applicable

• Conditions: trauma.; musculoskeletal sysytem and connective tissue diseases

• Registration Number: IRCT201112258104N4
• Lead Sponsor: researching center of Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

patients above 18 years old with trauma only to limbs and severe pain (VAS equal or above 6). stable vital signs including systolic blood pressure equal or above 90 mm HG ; pulse rate between 60 and 120 per minute ; O2 saturation equal or above 90%; GCS =15 ; no addiction to drugs ;no consumption opioids or analgesics before begining of study ;no history of leaver diseases ;renal diseases; respiratory diseases ;cardiovascular diseases ; psychiatric diseases,blood diseases .
Exclusion criteria: history of head trauma and contraindications for ketamine or morphine administration ; allergy to morphine or ketamine ; need to regional nerve block ; unable to conception of VAS;no interest to participate in study

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain control. Timepoint: 0, 10, 30, 60, 90 and 120 minutes after treatment. Method of measurement: Visual Analogous Scale (VAS).

Secondary Outcome Measures

Name	Time	Method
Side effects and changes in vital signs. Timepoint: 30 and 60 minutes after treatment. Method of measurement: Patient monitoring.