CompletedNot Applicable

Propofol Versus Sevoflurane on Acute Postoperative Pain

South Korea48 participantsStarted 2017-02-01

Plain-language 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 anesthesia.

Who can participate

Age range18 Years – 65 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * American Society of Anesthesiologists (ASA) I or II and aged 18-65 years for total shoulder arthroplasty Exclusion Criteria: * 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

What they're measuring

postoperative pain intensity

Timeframe: 24 hours after surgery

postoperative opioid consumption

Timeframe: 24 hours after surgery

Trial details

NCT IDNCT04333992

SponsorYeungnam University College of Medicine

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2017-12-12

View on ClinicalTrials.gov More Postoperative Pain trials