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NCT03539107 · ClinicalTrials.gov registry record · NA

Voiding Assessment Based on Minimum Spontaneous Void of 150 mL Compared to Retrograde Fill Method After Female Pelvic Floor Reconstructive Surgery

A NA study of Urinary Incontinence and Pelvic Organ Prolapse, sponsored by Yale University.

Completed
Registry status
NA
Development phase
110
Enrollment target
1
Study location

NCT03539107: Completed NA study of Urinary Incontinence and Pelvic Organ Prolapse, sponsored by Yale University.

NCT03539107 is a NA study of Urinary Incontinence and Pelvic Organ Prolapse that has completed, run by Yale University. The registered enrollment target is 110 participants, below the 260-participant average among 48 other Urinary Incontinence trials with a reported enrollment target (58% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03539107, a NA study of Urinary Incontinence and Pelvic Organ Prolapse, has completed, sponsored by Yale University.

COMPLETED
Registry status
NA
Development phase
110 participants
Enrollment target
1
Study location

Study Summary

This study will compare voiding assessment based on a minimum spontaneous voided volume of 150 cc with the standard retrograde fill approach in women after pelvic floor procedures.

Primary Outcome

The percentage of subjects who did not meet the required voiding assessment criteria and needed catheterization .

Interventions

  • PROCEDURE Retrograde bladder fill
  • OTHER spontaneous void

Study Locations (1)

Connecticut

  • Yale University - New Haven

Trial Details

FieldValue
Enrollment Target 110 participants
Start Date 2019-09-01
Est. Completion 2019-12-20
Phase NA
Yale University

1,492 total trials

What the finished NCT03539107 record still lists

NCT03539107 is an interventional study that assigns participants to a tested intervention. The registered 110 participants enrollment target is mid-sized for trials with a published cap, below the 260-participant average among 48 other Urinary Incontinence trials with a reported enrollment target (58% lower).

The record links to 2 conditions, with Urinary Incontinence appearing as the primary indexed condition, and to 2 interventions - of which Retrograde bladder fill is the first listed.

NCT03539107 reports a single indexed study location in Connecticut.

Frequently Asked Questions

What is clinical trial NCT03539107 about?

NCT03539107 is a clinical study titled "Voiding Assessment Based on Minimum Spontaneous Void of 150 mL Compared to Retrograde Fill Method After Female Pelvic Floor Reconstructive Surgery". This study will compare voiding assessment based on a minimum spontaneous voided volume of 150 cc with the standard retrograde fill approach in women after pelvic floor procedures.

What is the current status of trial NCT03539107?

This trial is currently completed. It is a NA study. The enrollment target is 110 participants. The study started on 2019-09-01. Estimated completion is 2019-12-20.

What conditions does trial NCT03539107 study?

This clinical trial studies the following conditions: Urinary Incontinence, Pelvic Organ Prolapse.

What interventions are being tested in trial NCT03539107?

The interventions under investigation include: Retrograde bladder fill (PROCEDURE), spontaneous void (OTHER).

Who is sponsoring clinical trial NCT03539107?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03539107 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Urinary Incontinence

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03539107's enrollment target sits among peer trials

110 23rd of 48 higher than 26 of 48 other Urinary Incontinence trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Urinary Incontinence trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03539107, the US trial registry maintained by the National Library of Medicine. NCT03539107 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.