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NCT00190606 · ClinicalTrials.gov registry record · Phase 2

Efficacy and Safety of Duloxetine, Placebo and Pelvic Floor Muscle Training in Subjects With Stress Urinary Incontinence

A Phase 2 study of Urinary Stress Incontinence, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 2
Development phase
200
Enrollment target
2
Study locations

NCT00190606 is a Phase 2 study of Urinary Stress Incontinence that has completed, run by Eli Lilly and Company. The registered enrollment target is 200 participants. The trial reports 2 study locations across 2 states.

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The verdict

NCT00190606, a Phase 2 study of Urinary Stress Incontinence, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 2
Development phase
200 participants
Enrollment target
2
Study locations

Study Summary

The study is a comparison of the efficacy and safety of duloxetine and pelvic floor muscle training with that of placebo in patients with moderate to severe stress urinary incontinence

Interventions

  • DRUG Duloxetine
  • DRUG placebo
  • PROCEDURE Pelvic Floor Muscle Training (PFMT)
  • PROCEDURE Imitation PFMT

Study Locations (2)

Florida

  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday - Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician - Weston

Other

  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday - Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician - Nieuwegein

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2002-01
Est. Completion 2006-04
Phase Phase 2

Sponsor

Eli Lilly and Company

1,341 total trials

What the Registry Record Tells You About NCT00190606

The ClinicalTrials.gov registry entry for NCT00190606 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Urinary Stress Incontinence appearing as the primary indexed condition, and to 4 interventions - of which Duloxetine is the first listed.

NCT00190606 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Florida, Other.

Frequently Asked Questions

What is clinical trial NCT00190606 about?

NCT00190606 is a clinical study titled "Efficacy and Safety of Duloxetine, Placebo and Pelvic Floor Muscle Training in Subjects With Stress Urinary Incontinence". The study is a comparison of the efficacy and safety of duloxetine and pelvic floor muscle training with that of placebo in patients with moderate to severe stress urinary incontinence

What is the current status of trial NCT00190606?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 200 participants. The study started on 2002-01. Estimated completion is 2006-04.

What conditions does trial NCT00190606 study?

This clinical trial studies the following conditions: Urinary Stress Incontinence.

What interventions are being tested in trial NCT00190606?

The interventions under investigation include: Duloxetine (DRUG), placebo (DRUG), Pelvic Floor Muscle Training (PFMT) (PROCEDURE), Imitation PFMT (PROCEDURE).

Who is sponsoring clinical trial NCT00190606?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00190606 being conducted?

This trial has 2 study locations across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.