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Clinical Trials/KCT0002246
KCT0002246
Completed
未知

The effect of intravenous dexmedetomidine versus propofol for postoperative analgesia in ankle surgery with spinal anesthesia

Samsung Medical Center0 sites44 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Samsung Medical Center
Enrollment
44
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients who performed a Arthroscopic debridement \& Brostrom operation under spinal anesthesia( 20 years or more, under 70 years)
  • ASA physical status I,II,III

Exclusion Criteria

  • Patients who refuse spinal anesthesia
  • Pateints who used opioids over a long period of time(30 mg/d of oral morphine or the equivalent) or had a serious side effect of opioid.
  • Pateints who have a history of serious side effect of dexmedetomidine or propofol
  • Patients who have significant coagulopathy or generalized infection
  • Patients with history of heart disease, liver or kidney dysfuncion
  • Patients who is unable to voluntarily agree to participate in the research

Outcomes

Primary Outcomes

Not specified

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