Overview

Comparison of Remimazolam and Dexmedetomidine for Intraoperative Sedation

Status:
Not yet recruiting
Trial end date:
2023-06-30
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to compare the sedation efficacy of dexmedetomidine and remimazolam for intraoperative sedation during regional block.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Seoul National University Hospital
Treatments:
Dexmedetomidine
Criteria
Inclusion Criteria:

- Patient scheduled for lower extremity surgery under regional anesthesia, aged 19-70,
of ASA class I or II.

Exclusion Criteria:

- Patient refusal

- Contraindications to regional or neuraxial anesthesia (patient refusal, increased
intracranial pressure, infection at puncture site, underlying neurologic disease,
severe hypovolemia, aortic or mitral stenosis, thrombocytopenia or coagulopathy)

- Contraindications to dexmedetomidine or remimazolam administration

- Allergy to dexmedetomidine or remimazolam

- Baseline MOAA/S score of 4 or less

- Pregnancy

- Other conditions considered unsuitable by the investigators