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A comparison of propofol vs. dexmedetomidine for sedation and contribution to perioperative analgesia for lumbar plexus block

Not Applicable
Conditions
hip osteoarthritis
Registration Number
JPRN-UMIN000023218
Lead Sponsor
Asahikawa Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
52
Inclusion Criteria

Not provided

Exclusion Criteria

Patients who have had alpha 2 agonist and/or antagonist, same side hip operation before the operation, anatomical abnormalities at their loins, neurological abnormalities, severe heart and/or renal failure, vasopressors in the operation, continuous unstable hemodynamic parameter (sBP>200, sBP<80, HR<40), disagreement with our study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain score(VAS) 24 hour after surgery
Secondary Outcome Measures
NameTimeMethod
Pain score(VAS) soon, 4 hour, and 48hour after surgery Timing of getting out of bed, satisfaction, the amount of analgesics
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