Trials / Recruiting
RecruitingNCT07125326
How the Method of Bladder Emptying After Epidural Placement in Labor Affects Postpartum Voiding
Intermittent Versus Continuous Bladder Catheterization in Epiduralized Laboring Patients: a Non-blinded Randomized Controlled Trial
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 564 (estimated)
- Sponsor
- University of Pittsburgh · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Detailed description
This is a randomized controlled trial to assess the effect of bladder catheterization method during labor with epidural anesthesia on the rate of postpartum urinary retention.
Conditions
- Urinary Retention
- Urinary Tract Infection (Diagnosis)
- Postpartum Acute Urinary Retention
- Postpartum Care
- Voiding Dysfunction
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Intermittent catheterization | intermittent bladder catheterization every four hours, or shorter intervals if volume exceeds 500mL per expert recommendation |
| PROCEDURE | Continuous catheterization | One catheter is placed in the bladder until pushing |
Timeline
- Start date
- 2025-12-09
- Primary completion
- 2026-08-01
- Completion
- 2027-08-01
- First posted
- 2025-08-15
- Last updated
- 2026-02-05
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT07125326. Inclusion in this directory is not an endorsement.