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Clinical Trials/NCT03341819
NCT03341819CompletedNot Applicable

Comparative Study Between Retained and Non-retained Urinary Catheter in Total Knee Arthorplasty With Epidural Anesthesia

Navamindradhiraj University2 sites in 1 country242 target enrollmentStarted: November 6, 2017Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
242
Locations
2
Primary Endpoint
postoperative urinary retention
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The purpose of this study is to compare the prevalence of postoperative urinary retention between retained and non-retained urinary catheter in total knee arthorplasty with epidural anesthesia

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
50 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Primary osteoarthritis of knee who were scheduled for a primary total knee arthroplasty

Exclusion Criteria

  • •History of renal disease
  • •History of urinary tract infection
  • •History of previous urinary tract surgery
  • •Benign prostatic hypertrophy
  • •Bilateral total knee arthroplasty
  • •Revision total knee arthroplasty
  • •Patients who need intraoperative monitoring of urine output

Outcomes

Primary Outcomes

postoperative urinary retention

Time Frame: 6 hours after surgery and 6 hours after remove urinary catherter

Patients who didn't void within 6 hours with suprapubic discomfort and had a urinary volume 400 mL or more confirmed by single intermittent catheterization

Secondary Outcomes

  • urinary tract infection(7 days after surgery)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Satit Thiengwittayaporn

Associate Professor

Navamindradhiraj University

Study Sites (2)

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