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Comparison effect of Apotel and Pergabalin in reduce pain after ?in orthopedic surgery ?

Phase 2
Recruiting
Conditions
pain after surgery.
Pain, not elsewhere classified
Registration Number
IRCT20141209020258N61
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
75
Inclusion Criteria

candidate orthopedic surgery ?lower limb
17 to 65 years
both of two gender

Exclusion Criteria

Coagulation disorders
Unwillingness to participate in the study
Severe hemodynamic instability
Hepatic, renal and cardiac disease
Sensitivity to Pregabalin and Apotel

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: We record pain in recovery, 2 and 12 and 24 hours after surgery. Method of measurement: Visual Analog Sacle.;Consumption of opioids. Timepoint: We record consumption of opioids in 24 hours in milligram. Method of measurement: milligram.;Sedation. Timepoint: We record ramsy sedation score in 24 hours after surgery.?. Method of measurement: ramsy sedation score.
Secondary Outcome Measures
NameTimeMethod
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