Status:
COMPLETED
Propofol Versus Sevoflurane on Acute Postoperative Pain
Lead Sponsor:
Yeungnam University College of Medicine
Conditions:
Postoperative Pain
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
This study was performed to compare the acute postoperative pain intensity and opioid consumption after total shoulder arthroplasty between propofol-remifentanil and sevoflurane-remifentanil anesthesi...
Detailed Description
After approval of the Institutional Review Board and written informed consent, 48 patients, aged 18-65 years for shoulder arthroplasty were enrolled in this prospective, randomized, double-blinded stu...
Eligibility Criteria
Inclusion
- American Society of Anesthesiologists (ASA) I or II and aged 18-65 years for total shoulder arthroplasty
Exclusion
- Use of routinely using analgesics, history of neurologic or psychologic disease, body mass index more than 35 kg/m2, and intake of any sedatives or analgesics within 24 h before surgery
Key Trial Info
Start Date :
February 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2018
Estimated Enrollment :
48 Patients enrolled
Trial Details
Trial ID
NCT04333992
Start Date
February 1 2017
End Date
January 1 2018
Last Update
April 3 2020
Active Locations (1)
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1
Eun kyung Choi
Daegu, Korea (the Republic Of), South Korea, 41944