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Clinical Trials/IRCT201209053104N2
IRCT201209053104N2
Completed
Phase 2

Comparing the effectiveness of adding paracetamol and dexamethasone to lidocaine for intravenous block of upper extremity on severity of pain and period ?of painless during and after surgery.?? ?

Vice chancellor for research, Kerman University of Medical Sciences0 sites60 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
IV Regional Anesthesia.
Sponsor
Vice chancellor for research, Kerman University of Medical Sciences
Enrollment
60
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Vice chancellor for research, Kerman University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • 20 to 60 years old; candidate for upper extremity surgery and ASA I or II.
  • Exclusion criteria:
  • Lidocaine allergy; infection; open fracture of limb; liver disease and addiction to opium and alcohol

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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