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Propofol Versus Sevoflurane on Acute Postoperative Pain

NCT04333992 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2020-04-03

No results posted yet for this study

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.

Conditions

  • Postoperative Pain

Interventions

DRUG

propofol and remifentanil

intravenous propofol and remifentanil using target-controlled infusion (TCI) devices

DRUG

sevoflurane and remifentanil

inhalator sevoflurane and remifentanil using target-controlled infusion (TCI) devices

Sponsors & Collaborators

  • Yeungnam University College of Medicine

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-01
Primary Completion
2017-12-12
Completion
2018-01-01

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04333992 on ClinicalTrials.gov