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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04954443
Other study ID # 084/2564
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2021
Est. completion date September 30, 2022

Study information

Verified date October 2022
Source Rajavithi Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date September 30, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 45 Years to 80 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Removing urinary catheter
Removing urinary catheter after vaginal surgery of pelvic organ prolapse

Locations

Country Name City State
Thailand Rajavithi Hospital Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Rajavithi Hospital

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Urinary retention Incident 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 Through study completion, an average of 1 year
Secondary Re-catheterization after removing urinary catheter Incident of re-catheterization after removing urinary catheter at 24 hour comparison with 48 hour after vaginal surgery of pelvic organ prolapse Through study completion, an average of 1 year
Secondary Urinary tract infection Incident 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 Through study completion, an average of 1 year
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