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
| Type | Name | Description |
|---|---|---|
| OTHER | Duration of Indwelling Catheter | Foley 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.