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Clinical Trials/KCT0005749
KCT0005749
Not yet recruiting
未知

The comparison of respiratory depression between propofol and propofol in combination with dexmedetomidine for deep sedation during total knee replacement under spinal anesthesia: a prospective randomized controlled trial

The Catholic University of Korea, Daejeon St. Mary's Hospital0 sites82 target enrollmentTBD
ConditionsNot Applicable

Overview

Phase
未知
Intervention
Not specified
Conditions
Not Applicable
Sponsor
The Catholic University of Korea, Daejeon St. Mary's Hospital
Enrollment
82
Status
Not yet recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
The Catholic University of Korea, Daejeon St. Mary's Hospital

Eligibility Criteria

Inclusion Criteria

  • American society of anesthesiology (ASA) physical status 1, 2, 3
  • Age: 50\-80 yrs
  • Patients for total knee replacement surgery under spinal anesthesia

Exclusion Criteria

  • Severe bradycardia, HR \<50 ?/min
  • Severe cardiopulmonary disease, ASA 4??
  • Severe hepatic or renal disease
  • Body mass index \> 35
  • contraindication to spinal anesthesia
  • Allergy to study medicine, propofol, dexmedetomidine
  • History of severe obstructive sleep apnea or a tendency for airway obstruction
  • Refusal of intraoperative sedation

Outcomes

Primary Outcomes

Not specified

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