Skip to content

Urinary Retention After Removing Urinary Catheter at 24 Hour Versus 48 Hour in Patients With Vaginal Surgery

Urinary Retention After Removing Urinary Catheter at 24 Hour Comparison With 48 Hour in Patients With Vaginal Surgery of Pelvic Organ Prolapse, Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04954443
Enrollment
60
Registered
2021-07-08
Start date
2021-07-01
Completion date
2022-09-30
Last updated
2022-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Organ Prolapse, Urinary Retention

Keywords

Urinary Retention, Pelvic Organ Prolapse, Vaginal surgery, Urinary catheter

Brief summary

Comparison incident of urinary retention in patients with vaginal surgery of pelvic organ prolapse, who removed urinary catheter at 24 hours versus 48 hours after surgery

Detailed description

Vaginal surgery of pelvic organ prolapse needs to insert urinary catheter for monitoring post-operative complication, hemodynamic status, and prevention post-operative urinary retention. Urinary retention occur 2.4 - 43% after pelvic organ prolapse surgery, whereas retaining urinary catheter is common cause of urinary tract infection, often hospital-acquired infection. At Rajavithi hospital always remove urinary catheter at 48 hour after surgery. Accordingly, appropriated time for removing urinary catheter in patients with vaginal surgery of pelvic organ prolapse is unclear. This study aims to reduce timing for removing urinary catheter after vaginal surgery, not increase urinary retention and re-catheterization and reduce urinary tract infection and day of hospital stay.

Interventions

PROCEDURERemoving urinary catheter

Removing urinary catheter after vaginal surgery of pelvic organ prolapse

Sponsors

Department of Medical Services Ministry of Public Health of Thailand
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Caregiver, Investigator)

Masking description

Single blind (Care provider, investigator)

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Woman with pelvic organ prolapse, who undergoing vaginal surgery and agrees to participate in this study * Able to understand and communicate Thai language

Exclusion criteria

* Woman with diabetes mellitus with HbA1C \> 10.9% * Woman with stroke * Woman with urinary tract infection before surgery * Woman with urinary retention before surgery * Woman, who experienced surgery for urinary incontinence * Woman, with operative complication including of hemorrhagic shock (Blood pressure \< 90/60 mmHg, Heart rate \> 120 beats per minute, Intra-operative blood loss \> or = 750 ml), urinary tract injury, bowel injury

Design outcomes

Primary

MeasureTime frameDescription
Urinary retentionThrough study completion, an average of 1 yearIncident of urinary retention (Post-void residual urine at least 150 ml) after removing urinary catheter at 24 hour comparison with 48 hour after vaginal surgery of pelvic organ prolapse

Secondary

MeasureTime frameDescription
Re-catheterization after removing urinary catheterThrough study completion, an average of 1 yearIncident of re-catheterization after removing urinary catheter at 24 hour comparison with 48 hour after vaginal surgery of pelvic organ prolapse
Urinary tract infectionThrough study completion, an average of 1 yearIncident of urinary tract infection (positive urine culture) after removing urinary catheter at 24 hour comparison with 48 hour after vaginal surgery of pelvic organ prolapse

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026