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NCT03373773 · ClinicalTrials.gov registry record · NA
Home vs. Office Foley Catheter Removal in Women With Voiding Difficulty Following Pelvic Reconstructive Surgery
A NA study, sponsored by Yale University.
- Completed
- Registry status
- NA
- Development phase
- 78
- Enrollment target
NCT03373773 is a NA study that has completed, run by Yale University. The registered enrollment target is 78 participants.
The verdict
NCT03373773, a NA study, has completed, sponsored by Yale University.
- COMPLETED
- Registry status
- NA
- Development phase
- 78 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the patient satisfaction with voiding assessment remotely after removal of Foley catheter at home by the patient or her caregiver compared to removal at the office by a healthcare provider in patients who have been diagnosed to have voiding difficulty after pelvic reconstructive surgery.
Interventions
- PROCEDURE Foley catheter removal
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 78 participants |
| Start Date | 2018-03-12 |
| Est. Completion | 2021-08-19 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03373773
The ClinicalTrials.gov registry entry for NCT03373773 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 78 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Yale University, which has 1,492 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Foley catheter removal is the first listed.
NCT03373773 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03373773 about?
NCT03373773 is a clinical study titled "Home vs. Office Foley Catheter Removal in Women With Voiding Difficulty Following Pelvic Reconstructive Surgery". The purpose of this study is to evaluate the patient satisfaction with voiding assessment remotely after removal of Foley catheter at home by the patient or her caregiver compared to removal at the office by a healthcare provider in patients who have been diagnosed to have voiding difficulty after p...
What is the current status of trial NCT03373773?
This trial is currently completed. It is a NA study. The enrollment target is 78 participants. The study started on 2018-03-12. Estimated completion is 2021-08-19.
What interventions are being tested in trial NCT03373773?
The interventions under investigation include: Foley catheter removal (PROCEDURE).
Who is sponsoring clinical trial NCT03373773?
This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.
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