Clinical Trials Directory

Trials / Terminated

TerminatedNCT04187365

Optimizing the Management of Postpartum Urinary Retention

Optimizing the Management of Postpartum Urinary Retention: Postpartum Urinary Retention (PUR) Study

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
70 (actual)
Sponsor
Northwestern University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

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.

Detailed description

The purpose of the study is to compare clinical outcomes of women with bladder distension injuries due to postpartum urinary retention (PUR) who have varying duration of catheterization for initial treatment of postpartum urinary retention. Hypotheses 1. Longer duration of therapeutic catheterization will be associated with resolution of postpartum voiding dysfunction in women who sustain severe bladder distension injuries due to postpartum urinary retention. Definition of resolution of postpartum voiding dysfunction: A. A post void residual volume of less than half of initial instilled volume on the first retrograde voiding trial, AND B. No need for re-treatment for urinary retention within 1 week 2. The incidence of postpartum urinary retention (PUR) will vary by route of delivery, with operative vaginal delivery having the highest incidence. 3. Risk factors for PUR will be related to intrapartum and delivery conditions

Conditions

Interventions

TypeNameDescription
OTHERDuration of Indwelling CatheterFoley catheter

Timeline

Start date
2019-11-22
Primary completion
2022-02-27
Completion
2022-02-27
First posted
2019-12-05
Last updated
2022-04-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04187365. Inclusion in this directory is not an endorsement.