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

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University of Pittsburgh

Status

Enrolling

Conditions

Urinary Tract Infection (Diagnosis)
Urinary Retention
Postpartum Care
Voiding Dysfunction
Postpartum Acute Urinary Retention

Treatments

Procedure: Intermittent catheterization
Procedure: Continuous catheterization

Study type

Interventional

Funder types

Other

Identifiers

NCT07125326
STUDY24030142

Details and patient eligibility

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.

Full 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.

Enrollment

564 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Pregnant patients planning vaginal delivery presenting in labor or for induction of labor
  • Age 18 years and older
  • Live fetus
  • Receive epidural anesthesia

Exclusion criteria

  • those under 18 years old
  • those with stillbirth
  • those with baseline overactive bladder symptoms, neurogenic bladder diagnoses, or otherwise using bladder catheterization during pregnancy

Patients will be excluded from UTI analyses if:

  • they received antibiotics intrapartum
  • had bacteriuria diagnosed by a clean catch specimen showing >100,000 CFU/mL of a single bacterial species, regardless of symptoms

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

564 participants in 2 patient groups

Intermittent catheterization
Active Comparator group
Treatment:
Procedure: Intermittent catheterization
Continuous catheterization
Active Comparator group
Treatment:
Procedure: Continuous catheterization

Trial contacts and locations

1

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Central trial contact

Anna Binstock, MD; Elena Lands, MD

Data sourced from clinicaltrials.gov

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