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NCT04090190 · ClinicalTrials.gov registry record · Phase 4

Inflammation in Women With Urgency Urinary Incontinence Treated With Anticholinergics

A Phase 4 study, sponsored by Brigham and Women's Hospital.

Completed
Registry status
Phase 4
Development phase
20
Enrollment target

NCT04090190: Completed Phase 4 study, sponsored by Brigham and Women's Hospital.

NCT04090190 is a Phase 4 study that has completed, run by Brigham and Women's Hospital. The registered enrollment target is 20 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04090190, a Phase 4 study, has completed, sponsored by Brigham and Women's Hospital.

COMPLETED
Registry status
Phase 4
Development phase
20 participants
Enrollment target

Study Summary

Urinary incontinence (UI) is a very common condition affecting women of all ages. The objective of this pilot study is to better understand the urinary microbiome and associated inflammatory markers in blood and urine in women with urgency UI. The study will assess how inflammation may affect response to standard of care anticholinergic medication treatment for urgency urinary incontinence.

Primary Outcome

Statistical testing was used to determine if there was a difference in inflammatory markers in the urine of patients between baseline visit and 6 week visit. 7 markers were chosen and compared, all inflammatory markers present in urine.

Interventions

  • DRUG Oxybutynin, Solifenacin, Tolterodine, Trospium, or Fesoterodine

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2019-10-30
Est. Completion 2021-10-31
Phase Phase 4
Brigham and Women's Hospital

937 total trials

What the finished NCT04090190 record still lists

NCT04090190 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which Oxybutynin, Solifenacin, Tolterodine, Trospium, or Fesoterodine is the first listed.

NCT04090190 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04090190 about?

NCT04090190 is a clinical study titled "Inflammation in Women With Urgency Urinary Incontinence Treated With Anticholinergics". Urinary incontinence (UI) is a very common condition affecting women of all ages. The objective of this pilot study is to better understand the urinary microbiome and associated inflammatory markers in blood and urine in women with urgency UI. The study will assess how inflammation may affect respon...

What is the current status of trial NCT04090190?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2019-10-30. Estimated completion is 2021-10-31.

What interventions are being tested in trial NCT04090190?

The interventions under investigation include: Oxybutynin, Solifenacin, Tolterodine, Trospium, or Fesoterodine (DRUG).

Who is sponsoring clinical trial NCT04090190?

This trial is sponsored by Brigham and Women's Hospital, which has 937 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04090190's enrollment target sits among peer trials

20 1753rd of 2000 higher than 167 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT04090190, the US trial registry maintained by the National Library of Medicine. NCT04090190 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.