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COMPLETED Phase 3

Evaluation of the Long- Term Effects of Spiriva on Lung Function in COPD Patients

NCT00144339 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this trial is to determine whether daily treatment with tiotropium (Spiriva®, Bromuro de Tiotropio®) inhalation capsule via HandiHaler® reduces the rate of decline in lung function over time in patients with COPD.

Interventions

  • DRUG placebo
  • DRUG tiotropium

Study Locations (20)

California

  • 205.235.3770 Boehringer Ingelheim Investigational Site — Carmichael
  • 205.235.3778 Boehringer Ingelheim Investigational Site — Escondito
  • 205.235.3810 Boehringer Ingelheim Investigational Site — Lakewood
  • 205.235.3758 Boehringer Ingelheim Investigational Site — Long Beach
  • 205.235.3812 Boehringer Ingelheim Investigational Site — Long Beach
  • 205.235.3773 Boehringer Ingelheim Investigational Site — Los Angeles
  • 205.235.3800 Boehringer Ingelheim Investigational Site — Los Angeles
  • 205.235.3802 Boehringer Ingelheim Investigational Site — Los Angeles
  • 205.235.3786 Pulmonary and Critical Care Medicine — Orange
  • 205.235.3811 Boehringer Ingelheim Investigational Site — Palo Alto
  • 205.235.3741 Boehringer Ingelheim Investigational Site — Rancho Mirage
  • 205.235.3717 Boehringer Ingelheim Investigational Site — San Diego
  • 205.235.3781 Boehringer Ingelheim Investigational Site — San Diego
  • 205.235.3784 Boehringer Ingelheim Investigational Site — San Diego
  • 205.235.3760 Boehringer Ingelheim Investigational Site — Sepulveda

Alabama

  • 205.235.3779 Boehringer Ingelheim Investigational Site — Anniston
  • 205.235.3785 Boehringer Ingelheim Investigational Site — Birmingham
  • 205.235.3804 Boehringer Ingelheim Investigational Site — Jasper
  • 205.235.3795 Boehringer Ingelheim Investigational Site — Mobile

Arizona

  • 205.235.3759 Boehringer Ingelheim Investigational Site — Phoenix

Trial Details

FieldValue
Enrollment Target 5,993 participants
Start Date 2002-12
Phase Phase 3

Sponsor

Boehringer Ingelheim

203 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00144339

The ClinicalTrials.gov registry entry for NCT00144339 describes a study currently listed as completed. It is categorized as Phase 3, 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 5,993 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boehringer Ingelheim, which has 203 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 Pulmonary Disease, Chronic Obstructive appearing as the primary indexed condition, and to 2 interventions — of which placebo 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: NCT00144339 reports 20 study locations spanning 3 distinct geographic areas — top geographies include California, Alabama, Arizona. 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 NCT00144339 about?

NCT00144339 is a clinical study titled "Evaluation of the Long- Term Effects of Spiriva on Lung Function in COPD Patients". The primary objective of this trial is to determine whether daily treatment with tiotropium (Spiriva®, Bromuro de Tiotropio®) inhalation capsule via HandiHaler® reduces the rate of decline in lung function over time in patients with COPD.

What is the current status of trial NCT00144339?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 5,993 participants. The study started on 2002-12.

What conditions does trial NCT00144339 study?

This clinical trial studies the following conditions: Pulmonary Disease, Chronic Obstructive. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00144339?

The interventions under investigation include: placebo (DRUG), tiotropium (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00144339?

This trial is sponsored by Boehringer Ingelheim, which has 203 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00144339 being conducted?

This trial has 20 study locations across Alabama, Arizona, California. 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