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Effect of intravenous Ketamine in reducing postoperative pai

Phase 3
Recruiting
Conditions
ower limb fracture.
Lower limb fracture
Registration Number
IRCT20221029056333N1
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
88
Inclusion Criteria

Age 20 to 60 years old
Lower limb fracture
Having consent to enter the study

Exclusion Criteria

Patients with a history of psychosis and cognitive disorders
Patients with a history of drug addiction
Pregnant women

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: In 5 recovery periods, 6 hours, 12 hours and 24 hours after surgery. Method of measurement: Using the VAS scale & record severe pain intensity.
Secondary Outcome Measures
NameTimeMethod
ausea. Timepoint: 24 hours after surgery. Method of measurement: By N&V benchmark.;Vomiting. Timepoint: 24 hours after surgery. Method of measurement: By N&V benchmark.
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