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NCT07125326 · ClinicalTrials.gov registry record · NA
How the Method of Bladder Emptying After Epidural Placement in Labor Affects Postpartum Voiding
A NA study of Urinary Retention and Urinary Tract Infection (Diagnosis), sponsored by University of Pittsburgh.
- Recruiting
- Registry status
- NA
- Development phase
- 564
- Enrollment target
- 1
- Study location
NCT07125326: Recruiting NA study of Urinary Retention and Urinary Tract Infection (Diagnosis), sponsored by University of Pittsburgh.
NCT07125326 is a NA study of Urinary Retention and Urinary Tract Infection (Diagnosis) that is actively recruiting participants, run by University of Pittsburgh. The registered enrollment target is 564 participants, above the 89-participant average among 11 other Urinary Retention trials with a reported enrollment target (534% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07125326, a NA study of Urinary Retention and Urinary Tract Infection (Diagnosis), is actively recruiting participants, sponsored by University of Pittsburgh.
- RECRUITING
- Registry status
- NA
- Development phase
- 564 participants
- Enrollment target
- 1
- Study location
Study Summary
At least ten percent of patients have postpartum urinary retention or difficulty urinating after birth, which can cause incontinence and other urinary problems long-term. After getting an epidural placed, patients should be numb in their pelvic region. This numbness makes it difficult to feel the need to urinate, so patients need a urinary catheter placed to empty the bladder. Some patients have one catheter placed throughout their labor and others have a catheter placed to empty the bladder then removed every few hours. The investigators are studying whether placing a catheter once or catheterizing multiple times affects the rate of postpartum urinary problems and infection.
Primary Outcome
Urinary retention defined as overt inability to void at six hours after last bladder emptying postpartum or symptomatic incomplete emptying, or covert retention of \>150cc urine in the bladder after voiding Collecting number of participants who experience this
Conditions Studied
Interventions
- PROCEDURE Intermittent catheterization
- PROCEDURE Continuous catheterization
Study Locations (1)
Pennsylvania
- UPMC Magee-Womens Hospital - Pittsburgh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 564 participants |
| Start Date | 2025-12-09 |
| Est. Completion | 2027-08 |
| Phase | NA |
What NCT07125326 shows while recruiting
NCT07125326 is an interventional study that assigns participants to a tested intervention. The registered 564 participants enrollment target is mid-sized for trials with a published cap, above the 89-participant average among 11 other Urinary Retention trials with a reported enrollment target (534% higher).
The record links to 5 conditions, with Urinary Retention appearing as the primary indexed condition, and to 2 interventions - of which Intermittent catheterization is the first listed.
NCT07125326 reports a single indexed study location in Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT07125326 about?
NCT07125326 is a clinical study titled "How the Method of Bladder Emptying After Epidural Placement in Labor Affects Postpartum Voiding". At least ten percent of patients have postpartum urinary retention or difficulty urinating after birth, which can cause incontinence and other urinary problems long-term. After getting an epidural placed, patients should be numb in their pelvic region. This numbness makes it difficult to feel the ne...
What is the current status of trial NCT07125326?
This trial is currently recruiting. It is a NA study. The enrollment target is 564 participants. The study started on 2025-12-09. Estimated completion is 2027-08.
What conditions does trial NCT07125326 study?
This clinical trial studies the following conditions: Urinary Retention, Urinary Tract Infection (Diagnosis), Postpartum Care, Voiding Dysfunction, Postpartum Acute Urinary Retention.
What interventions are being tested in trial NCT07125326?
The interventions under investigation include: Intermittent catheterization (PROCEDURE), Continuous catheterization (PROCEDURE).
Who is sponsoring clinical trial NCT07125326?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07125326 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Urinary Retention
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT07125326's enrollment target sits among peer trials
564 1st of 11 higher than 11 of 11 other Urinary Retention trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Urinary Retention trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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