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Clinical Trials/NCT03746444
NCT03746444
Unknown
Not Applicable

Comparison of Effects of Combined Spinoepidural and General Anesthesia Effects on Incidence of Postoperative Complications Following Total Knee Arthroplasty

Ufuk University1 site in 1 country130 target enrollmentNovember 20, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Arthroplasty, Replacement, Knee
Sponsor
Ufuk University
Enrollment
130
Locations
1
Primary Endpoint
Death
Last Updated
7 years ago

Overview

Brief Summary

The aim of this study is to investigate the effect of combined spinoepidural and general anesthesia on the incidence of postoperative complications following total knee arthroplasty

Detailed Description

Total knee arthroplasty is known to cause complications (pulmonary thromboembolism, acute kidney injury, arryhthmias and infection). The investigators aimed to study the effects of two different anesthesia techniques, i.e. combined spinoepidural anesthesia and general anesthesia on the incidence of postoperative complications such as arrhythmia, pulmonary thrombeoembolism, infection, acute kidney injury and mortality.

Registry
clinicaltrials.gov
Start Date
November 20, 2018
End Date
December 25, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Ufuk University
Responsible Party
Principal Investigator
Principal Investigator

Perihan Ekmekçi

Primary Investigator

Ufuk University

Eligibility Criteria

Inclusion Criteria

  • Patients scheduled to undergo elective unilateral total knee arthroplasty

Exclusion Criteria

  • Patient refusal
  • Scheduled for bilateral or unilateral unicondylar knee arthroplasty
  • Known history of allergy to drugs used in the study
  • Severe systemic disease
  • Morbid obesity (BMI\>30)
  • History of renal dysfunction

Outcomes

Primary Outcomes

Death

Time Frame: Postoperative sixth week

Number of participants with mortality

Pulmonary Thromboembolism

Time Frame: Postoperative sixth week

Number of participants with new onset pulmonary thromboembolism

Infection

Time Frame: Postoperative sixth week

Number of participants with new onset infection

Arryhthmia

Time Frame: Postoperative sixth week

Number of participants with new onset arryhthmia requiring treatment

Acute Kidney Injury

Time Frame: Postoperative sixth week

Number of participants with new onset acute kidney injury

Study Sites (1)

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