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Comparison · NCT01923129-ff83d0b2

24 Hour Postop Catheter Removal vs 72 Hour Postoperative Catheter Removal: Number of Participants With a Symptomatic Urinary Tract Infection

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. 24 Hour Postop Catheter Removal vs 72 Hour Postoperative Catheter Removal: Number of Participants With a Symptomatic Urinary Tract Infection. Trial comparisons, record NCT01923129-ff83d0b2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01923129-ff83d0b2

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 1000.0513wilson
Risk in group 20.1130.05820.207wilson
Risk difference, group 1 minus group 2-0.113-0.207-0.0378newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one fewer participant with the outcome on 24 Hour Postop Catheter Removal than on 72 Hour Postoperative Catheter Removal8.884.8326.4from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 124 Hour Postop Catheter Removal
group will receive the study medication prazosin ( 1 mg PO) 6 hours prior to catheter discontinuation (24 hours postoperatively)~Prazosin given 6 hours prior to catheter removal in the 24 hour group: Prazosin given orally (1 mg) 6 hours prior to catheter removal (hour 18 postoperatively)
071OG000
Group 272 Hour Postoperative Catheter Removalcatheter removed on postoperative day 3 (72 hours postoperatively)871OG001

Outcome

Type
SECONDARY
Title
Number of Participants With a Symptomatic Urinary Tract Infection
Description
Urinary tract infection defined as symptomatic urinary complaints such as dysuria, with urinalysis consistent with infection.
Time frame
During 1 week of hospitalization (prior to discharge)
Population

Source ClinicalTrials.gov

Trial

Title
Optimal Duration of Indwelling Urinary Catheter Following Pelvic Surgery
NCT number
NCT01923129
Phases
NA
Conditions
Urinary Retention
Interventions
Prazosin given 6 hours prior to catheter removal in the 24 hour group
Lead sponsor
Cedars-Sinai Medical Center
Results first posted
2019-02-20

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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