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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT05538273
Other study ID # 1946054-1
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date September 8, 2022
Est. completion date March 14, 2023

Study information

Verified date March 2023
Source WellSpan Health
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a combined retrospective observational study that will collect data on urinary catheter removal of patients who underwent pelvic surgery by a gynecologic oncologist to assess timing safety and its implications in postoperative care.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date March 14, 2023
Est. primary completion date March 14, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age above 18 - female gender - undergoing pelvic surgery for benign or malignant indications by a gynecologic oncologist Exclusion Criteria: - Age less than 18 years of age at the time of surgery - pregnant - individual is a prisoner

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Early removal of urinary catheter postoperatively
removal of urinary catheter less than 24 hours after surgery
Late removal of urinary catheter postoperatively
removal of urinary catheter greater than 24 hours after surgery

Locations

Country Name City State
United States WellSpan York Hospital York Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
WellSpan Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Urinary retention rate after urinary catheter removal postoperatively urinary retention rate will be measured as need for re-catheterization postoperatively 30 days after surgery
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