Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07125326

How the Method of Bladder Emptying After Epidural Placement in Labor Affects Postpartum Voiding

Led by University of Pittsburgh · Updated on 2026-02-05

564

Participants Needed

1

Research Sites

85 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

How the Method of Bladder Emptying After Epidural Placement in Labor Affects Postpartum Voiding

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant patients planning vaginal delivery presenting in labor or for induction of labor
  • Age 18 years and older
  • Live fetus
  • Receive epidural anesthesia
Not Eligible

You will not qualify if you...

  • Under 18 years old
  • Stillbirth
  • Baseline overactive bladder symptoms, neurogenic bladder diagnoses, or use of bladder catheterization during pregnancy
  • Received antibiotics during labor
  • Diagnosed bacteriuria with >100,000 CFU/mL of a single bacterial species in urine, regardless of symptoms

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UPMC Magee-Womens Hospital

Pittsburgh, Pennsylvania, United States, 15217

Actively Recruiting

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Research Team

E

Elena Lands, MD

CONTACT

A

Anna Binstock, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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