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COMPLETED Phase 4

Effect and Safety Of Detrol LA In Men With Overactive Bladder Symptoms With Or Without Bladder Outlet Obstruction

NCT00147654 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of the trial is to evaluate the effect of tolterodine ER plus tamsulosin versus placebo on patient perception of overall treatment benefit in men who have frequency and urgency, with or without urinary urge incontinence (UUI), with or without bladder outlet obstruction (BOO).

Conditions Studied

Interventions

  • DRUG Tolterodine ER 4 mg QD
  • DRUG Tamsulosin 0.4 mg QD

Study Locations (20)

California

  • Pfizer Investigational Site — Anaheim
  • Pfizer Investigational Site — Culver City
  • Pfizer Investigational Site — Fresno
  • Pfizer Investigational Site — La Mesa
  • Pfizer Investigational Site — Long Beach
  • Pfizer Investigational Site — Los Angeles
  • Pfizer Investigational Site — Murrieta
  • Pfizer Investigational Site — Poway
  • Pfizer Investigational Site — San Bernardino
  • Pfizer Investigational Site — Santa Monica

Colorado

  • Pfizer Investigational Site — Aurora
  • Pfizer Investigational Site — Boulder
  • Pfizer Investigational Site — Denver

Alabama

  • Pfizer Investigational Site — Birmingham
  • Pfizer Investigational Site — Homewood

Connecticut

  • Pfizer Investigational Site — New Britain
  • Pfizer Investigational Site — Waterbury

Florida

  • Pfizer Investigational Site — Melbourne
  • Pfizer Investigational Site — Ocala

Arizona

  • Pfizer Investigational Site — Tucson

Trial Details

FieldValue
Enrollment Target 830 participants
Start Date 2004-11
Est. Completion 2006-05
Phase Phase 4

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00147654

The ClinicalTrials.gov registry entry for NCT00147654 describes a study currently listed as completed. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 830 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer's Upjohn has merged with Mylan to form Viatris, which has 27 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Urinary Incontinence appearing as the primary indexed condition, and to 2 interventions — of which Tolterodine ER 4 mg QD is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00147654 reports 20 study locations spanning 6 distinct geographic areas — top geographies include California, Colorado, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00147654 about?

NCT00147654 is a clinical study titled "Effect and Safety Of Detrol LA In Men With Overactive Bladder Symptoms With Or Without Bladder Outlet Obstruction". The primary objective of the trial is to evaluate the effect of tolterodine ER plus tamsulosin versus placebo on patient perception of overall treatment benefit in men who have frequency and urgency, with or without urinary urge incontinence (UUI), with or without bladder outlet obstruction (BOO).

What is the current status of trial NCT00147654?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 830 participants. The study started on 2004-11. Estimated completion is 2006-05.

What conditions does trial NCT00147654 study?

This clinical trial studies the following conditions: Urinary Incontinence. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00147654?

The interventions under investigation include: Tolterodine ER 4 mg QD (DRUG), Tamsulosin 0.4 mg QD (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00147654?

This trial is sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris, which has 27 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00147654 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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