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NCT01479816 · ClinicalTrials.gov registry record

Urinary Continence Index for Prediction of Urinary Incontinence in Older Women

A clinical trial of Urinary Incontinence, sponsored by Ananias Diokno.

Completed
Registry status
702
Enrollment target
2
Study locations

NCT01479816: Completed study of Urinary Incontinence, sponsored by Ananias Diokno.

NCT01479816 is a study of Urinary Incontinence that has completed, run by Ananias Diokno. The registered enrollment target is 702 participants, above the 247-participant average among 48 other Urinary Incontinence trials with a reported enrollment target (184% higher). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01479816, a study of Urinary Incontinence, has completed, sponsored by Ananias Diokno.

COMPLETED
Registry status
702 participants
Enrollment target
2
Study locations

Study Summary

This study will analyse existing data to establish a clinically useful index to predict those women who are more likely to become incontinent. This would create significant opportunities for focused prevention and early intervention strategies.

Primary Outcome

Several risk factors identified can serve as an index in predicting the development of urinary incontinence in elderly women.

Conditions Studied

Study Locations (2)

Michigan

  • Oakland University - Rochester
  • William Beaumont Hospital - Royal Oak

Trial Details

FieldValue
Enrollment Target 702 participants
Start Date 2011-09
Est. Completion 2015-12
Ananias Diokno

2 total trials

What the finished NCT01479816 record still lists

NCT01479816 is an observational study that tracks outcomes without assigning an intervention. The registered 702 participants enrollment target is mid-sized for trials with a published cap, above the 247-participant average among 48 other Urinary Incontinence trials with a reported enrollment target (184% higher).

The record links to 1 condition, with Urinary Incontinence appearing as the primary indexed condition, and to 0 interventions.

NCT01479816 reports a single indexed study location in Michigan.

Frequently Asked Questions

What is clinical trial NCT01479816 about?

NCT01479816 is a clinical study titled "Urinary Continence Index for Prediction of Urinary Incontinence in Older Women". This study will analyse existing data to establish a clinically useful index to predict those women who are more likely to become incontinent. This would create significant opportunities for focused prevention and early intervention strategies.

What is the current status of trial NCT01479816?

This trial is currently completed. The enrollment target is 702 participants. The study started on 2011-09. Estimated completion is 2015-12.

What conditions does trial NCT01479816 study?

This clinical trial studies the following conditions: Urinary Incontinence.

Who is sponsoring clinical trial NCT01479816?

This trial is sponsored by Ananias Diokno, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01479816 being conducted?

This trial has 2 study locations across Michigan. 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 NCT01479816's enrollment target sits among peer trials

702 5th of 48 higher than 44 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 NCT01479816, the US trial registry maintained by the National Library of Medicine. NCT01479816 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.