Trial · NCT01923129
Optimal Duration of Indwelling Urinary Catheter Following Pelvic Surgery
NCT01923129, Not applicable, Completed, Cedars-Sinai Medical Center; results first posted 2019-02-20
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Optimal Duration of Indwelling Urinary Catheter Following Pelvic Surgery. Trials, record NCT01923129. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01923129
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Optimal Duration of Indwelling Urinary Catheter Following Pelvic Surgery
- NCT number
- NCT01923129
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 142 participants, actual
- Lead sponsor
- Cedars-Sinai Medical Center
- Conditions
- Urinary Retention
- Interventions
- Prazosin given 6 hours prior to catheter removal in the 24 hour group
- First posted
- 2013-08-15
- Last updated
- 2019-02-20
- Results first posted
- 2019-02-20
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of Participants With Acute Urinary Retention | Postoperative day 1 or postpoperative 3 depending on group randomization | Acute urinary retention will be defined as catheter discontinuation with inability to void 6 hours post-removal, or void with post-void residual greater than 200 cc of urine. |
| Secondary | Number of Participants With a Symptomatic Urinary Tract Infection | During 1 week of hospitalization (prior to discharge) | Urinary tract infection defined as symptomatic urinary complaints such as dysuria, with urinalysis consistent with infection. |
Source ClinicalTrials.gov
Outcomes2
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Participants With Acute Urinary Retention | Postoperative day 1 or postpoperative 3 depending on group randomization | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Participants With a Symptomatic Urinary Tract Infection | During 1 week of hospitalization (prior to discharge) | Participants | COUNT_OF_PARTICIPANTS |
Source ClinicalTrials.gov
Results by group4
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Participants With Acute Urinary Retention | 24 Hour Postop Catheter Removal | 6 | Participants | ||
| Number of Participants With Acute Urinary Retention | 72 Hour Postoperative Catheter Removal | 7 | Participants | ||
| Number of Participants With a Symptomatic Urinary Tract Infection | 24 Hour Postop Catheter Removal | 0 | Participants | ||
| Number of Participants With a Symptomatic Urinary Tract Infection | 72 Hour Postoperative Catheter Removal | 8 | Participants |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | 24 Hour Postop Catheter Removal | 71 | |
| Overall Study | STARTED | 72 Hour Postoperative Catheter Removal | 71 | |
| Overall Study | COMPLETED | 24 Hour Postop Catheter Removal | 71 | |
| Overall Study | COMPLETED | 72 Hour Postoperative Catheter Removal | 71 | |
| Overall Study | NOT COMPLETED | 24 Hour Postop Catheter Removal | 0 | |
| Overall Study | NOT COMPLETED | 72 Hour Postoperative Catheter Removal | 0 |
Source ClinicalTrials.gov
Adverse events2
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Dizziness | Cardiac disorders | 24 Hour Postop Catheter Removal | 6 | 71 | 6 |
| other | Dizziness | Cardiac disorders | 72 Hour Postoperative Catheter Removal | 0 | 71 | 0 |
Source ClinicalTrials.gov
Adverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | 24 Hour Postop Catheter Removal | 0 | 71 |
| Total, all-cause mortality | 72 Hour Postoperative Catheter Removal | 0 | 71 |
| Total, other adverse events | 24 Hour Postop Catheter Removal | 6 | 71 |
| Total, other adverse events | 72 Hour Postoperative Catheter Removal | 0 | 71 |
| Total, serious adverse events | 24 Hour Postop Catheter Removal | 0 | 71 |
| Total, serious adverse events | 72 Hour Postoperative Catheter Removal | 0 | 71 |
Source ClinicalTrials.gov
Papers2
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons4
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| 24 Hour Postop Catheter Removal vs 72 Hour Postoperative Catheter Removal: Number of Participants With Acute Urinary Retention | Trial comparisons |
| 24 Hour Postop Catheter Removal vs 72 Hour Postoperative Catheter Removal: deaths from any cause | Trial comparisons |
| 24 Hour Postop Catheter Removal vs 72 Hour Postoperative Catheter Removal: Number of Participants With a Symptomatic Urinary Tract Infection | Trial comparisons |
| 24 Hour Postop Catheter Removal vs 72 Hour Postoperative Catheter Removal: serious adverse events | Trial comparisons |
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
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
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT01923129
GET https://conductscience.org/api/trials/v1/NCT01923129/registered