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Investigation of the effect of Ketamine in comparison with Dexmedetomidine dose in pain management and postoperative complications of orthopedics

Phase 3
Recruiting
Conditions
femoral fracture
Femoral orthopedic surgery.
Registration Number
IRCT20161014030294N5
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
70
Inclusion Criteria

Age 18 to 65 years
orthopedic surgery of the lower limb or pelvis with general anesthesia
consent to research
absence of underlying diseases such as cardiovascular
physical condition 1 and 2 American Society of Anesthesiologists (ASA)

Exclusion Criteria

Hypersensitivity to Ketamine or Dexmedetomidine
cardiovascular and pulmonary disease
death of patient
dissatisfaction with participation in the study
withdrawal from the study at any stage

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The extent of postoperative pain. Timepoint: Pain score before the intervention and after up to 8 hours after the operation every hour. Method of measurement: VAS scale.
Secondary Outcome Measures
NameTimeMethod
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