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Clinical Trials/NCT06344884
NCT06344884CompletedNot Applicable

Early Patient Removal of Urinary Catheters After Urogynecologic Surgery

University of North Carolina, Chapel Hill1 site in 1 country128 target enrollmentStarted: June 24, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
128
Locations
1
Primary Endpoint
Number of patients with ongoing urinary retention (noninferiority)

Study Overview

Brief Summary

Management of postoperative urinary retention often requires the use of indwelling catheters. In a previous study, the investigators determined that patient removal of catheters at home is non-inferior to standard office removal on postoperative day three or four (POD3-4). The purpose of this study is to determine whether patient removal of catheters at home on postoperative day one (POD1) is noninferior to removal on POD 3-4.

Detailed Description

Randomized, controlled, non-inferiority trial to compare the risk of urinary retention between patient urinary catheter removal on POD1 versus POD3-4 after urogynecologic surgery.

Aim One: Is the risk of urinary retention non-inferior with patient removal of transurethral catheters on POD1 versus POD3-4 after urogynecologic surgery?

Aim Two: Does healthcare resource utilization (nursing calls, patient messages, and office visits) differ between patient removal of transurethral catheters on POD1 versus POD3-4?

Aim Three: Does the patient experience differ between patient removal of transurethral catheters on POD1 versus POD3-4?

Aim Four: Does the incidence of postoperative UTI differ between patient removal of transurethral catheters on POD1 versus POD3-4?

Study Design

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

Eligibility Criteria

Ages
18 Years to 99 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •All women undergoing prolapse or anti-incontinence surgery who fail their voiding trials prior to discharge.

Exclusion Criteria

  • •Non-English speaking (due to limited resources to consent non-English speaking patients)
  • •Postvoid residual (PVR) >150 mL or dependent upon catheterization to void pre-operatively
  • •Intra-operative complication requiring prolonged catheterization

Arms & Interventions

Standard Catheter Removal

No Intervention

Participants in this arm will be asked to remove their catheters POD3-4.

Early Catheter Removal

Experimental

Participants in this arm will be asked to remove their catheters POD1.

Intervention: Early catheter removal (Procedure)

Outcomes

Primary Outcomes

Number of patients with ongoing urinary retention (noninferiority)

Time Frame: From Postoperative day 1 through postoperative week 8

Defined as need for catheter replacement or clean intermittent self catheterization (CISC) after catheter removal on POD1 vs POD3-4. A 95% confidence interval of the difference in proportions between the two groups will be used to assess the tenability of a non-inferiority proposition.

Secondary Outcomes

  • Total patient contacts for voiding dysfunction Combined(From Postoperative day 1 through postoperative week 8)
  • Number of patients with ongoing urinary retention(From Postoperative day 1 through postoperative week 8)
  • Number of patients treated for postoperative UTI.(From Postoperative day 1 through postoperative week 8)
  • Number of patient contacts for voiding dysfunction by Type(From Postoperative day 1 through postoperative week 8)
  • Patient Satisfaction Survey Score-Satisfaction(Postoperative week 2)
  • Patient Satisfaction Survey Score-Pain(Postoperative week 2)
  • Patient Satisfaction Survey Score-Ease of Use(Postoperative week 2)
  • Patient Satisfaction Survey Score-Likelihood to Use Again(Postoperative week 2)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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