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Optimizing the Management of Postpartum Urinary Retention

NCT04187365 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2022-04-20

No results posted yet for this study

Summary

A study aimed at characterizing the comparing duration of catheterization for treatment of postpartum urinary retention (PUR) and characterizing short and long-term pelvic floor symptoms in women who have PUR.

Conditions

  • Urinary Retention

Interventions

OTHER

Duration of Indwelling Catheter

Foley catheter

Sponsors & Collaborators

Principal Investigators

  • Sarah Collins, MD · Northwestern University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-11-22
Primary Completion
2022-02-27
Completion
2022-02-27

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04187365 on ClinicalTrials.gov