Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00171184 · ClinicalTrials.gov registry record · Phase 4

Efficacy, Safety, and Tolerability of Darifenacin in Patients Aged > 65 Years With Overactive Bladder

A Phase 4 study of Overactive Bladder, sponsored by Novartis.

Completed
Registry status
Phase 4
Development phase
400
Enrollment target
1
Study location

NCT00171184 is a Phase 4 study of Overactive Bladder that has completed, run by Novartis. The registered enrollment target is 400 participants, above the 203-participant average among 45 other Overactive Bladder trials with a reported enrollment target (97% higher). The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00171184, a Phase 4 study of Overactive Bladder, has completed, sponsored by Novartis.

COMPLETED
Registry status
Phase 4
Development phase
400 participants
Enrollment target
1
Study location

Study Summary

The objective of this study is to assess the efficacy, safety and tolerability of 12-weeks treatment with darifenacin in patients aged \>Ý 65 years with OAB.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Darifenacin

Study Locations (1)

Texas

  • Scott Department of Urology Baylor College of Medicine - Houston

Trial Details

FieldValue
Enrollment Target 400 participants
Start Date 2005-04
Est. Completion 2006-06
Phase Phase 4

Sponsor

Novartis

265 total trials

What the Registry Record Tells You About NCT00171184

The ClinicalTrials.gov registry entry for NCT00171184 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 203-participant average among 45 other Overactive Bladder trials with a reported enrollment target (97% higher). The listed sponsor is Novartis, which has 265 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Overactive Bladder appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT00171184 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT00171184 about?

NCT00171184 is a clinical study titled "Efficacy, Safety, and Tolerability of Darifenacin in Patients Aged > 65 Years With Overactive Bladder". The objective of this study is to assess the efficacy, safety and tolerability of 12-weeks treatment with darifenacin in patients aged \>Ý 65 years with OAB.

What is the current status of trial NCT00171184?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 400 participants. The study started on 2005-04. Estimated completion is 2006-06.

What conditions does trial NCT00171184 study?

This clinical trial studies the following conditions: Overactive Bladder.

What interventions are being tested in trial NCT00171184?

The interventions under investigation include: Placebo (DRUG), Darifenacin (DRUG).

Who is sponsoring clinical trial NCT00171184?

This trial is sponsored by Novartis, which has 265 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00171184 being conducted?

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

Similar trials for Overactive Bladder

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.

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

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.