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Completed Phase 4 Interventional Results available

Investigate the Impact of Early Treatment Initiation With Tiotropium in Patients Recovering From Hospitalization for an Acute COPD Exacerbation 1

ClinicalTrials.gov ID: NCT01663987

Public ClinicalTrials.gov record NCT01663987. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 5:47 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Placebo-controlled, Double-blind, Parallel Group, Multi Center Study to Assess the Safety and Efficacy of Tiotropium Bromide (18 µg) Delivered Via the HandiHaler® in Chronic Obstructive Pulmonary Disease (COPD) Subjects Recovering From Hospitalization for an Acute Exacerbation (Hospital Discharge Study 1)

Study identification

NCT ID
NCT01663987
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
79 participants

Conditions and interventions

Interventions

  • tiotropium bromide Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2012
Primary completion
Apr 30, 2014
Completion
Apr 30, 2014
Last update posted
Oct 16, 2018

2012 – 2014

United States locations

U.S. sites
49
U.S. states
20
U.S. cities
47
Facility City State ZIP Site status
205.477.001039 Boehringer Ingelheim Investigational Site Birmingham Alabama
205.477.001050 Boehringer Ingelheim Investigational Site Birmingham Alabama
205.477.001021 Boehringer Ingelheim Investigational Site Florence Alabama
205.477.001046 Boehringer Ingelheim Investigational Site Fountain Valley California
205.477.001052 Boehringer Ingelheim Investigational Site Sacramento California
205.477.001059 Boehringer Ingelheim Investigational Site San Diego California
205.477.001009 Boehringer Ingelheim Investigational Site Stamford Connecticut
205.477.001040 Boehringer Ingelheim Investigational Site Waterbury Connecticut
205.477.001051 Boehringer Ingelheim Investigational Site Brandon Florida
205.477.001044 Boehringer Ingelheim Investigational Site Clearwater Florida
205.477.001037 Boehringer Ingelheim Investigational Site Eustis Florida
205.477.001017 Boehringer Ingelheim Investigational Site Miami Florida
205.477.001063 Boehringer Ingelheim Investigational Site Miami Florida
205.477.001001 Boehringer Ingelheim Investigational Site St. Petersburg Florida
205.477.001004 Boehringer Ingelheim Investigational Site Decatur Georgia
205.477.001012 Boehringer Ingelheim Investigational Site Duluth Georgia
205.477.001064 Boehringer Ingelheim Investigational Site Belleville Illinois
205.477.001038 Boehringer Ingelheim Investigational Site Muncie Indiana
205.477.001007 Boehringer Ingelheim Investigational Site Baltimore Maryland
205.477.001014 Boehringer Ingelheim Investigational Site Columbia Maryland
205.477.001018 Boehringer Ingelheim Investigational Site Livonia Michigan
205.477.001068 Boehringer Ingelheim Investigational Site Union New Jersey
205.477.001035 Boehringer Ingelheim Investigational Site Cooperstown New York
205.477.001023 Boehringer Ingelheim Investigational Site New York New York
205.477.001061 Boehringer Ingelheim Investigational Site Staten Island New York
205.477.001027 Boehringer Ingelheim Investigational Site Burlington North Carolina
205.477.001032 Boehringer Ingelheim Investigational Site Huntersville North Carolina
205.477.001020 Boehringer Ingelheim Investigational Site Seneca North Carolina
205.477.001034 Boehringer Ingelheim Investigational Site Cincinnati Ohio
205.477.001053 Boehringer Ingelheim Investigational Site Columbus Ohio
205.477.001011 Boehringer Ingelheim Investigational Site Dayton Ohio
205.477.001057 Boehringer Ingelheim Investigational Site Tulsa Oklahoma
205.477.001006 Boehringer Ingelheim Investigational Site Portland Oregon
205.477.001083 Boehringer Ingelheim Investigational Site Downingtown Pennsylvania
205.477.001031 Boehringer Ingelheim Investigational Site Monroeville Pennsylvania
205.477.001028 Boehringer Ingelheim Investigational Site Anderson South Carolina
205.477.001019 Boehringer Ingelheim Investigational Site Charleston South Carolina
205.477.001010 Boehringer Ingelheim Investigational Site Fort Mill South Carolina
205.477.001025 Boehringer Ingelheim Investigational Site Gaffney South Carolina
205.477.001002 Boehringer Ingelheim Investigational Site Rock Hill South Carolina
205.477.001026 Boehringer Ingelheim Investigational Site Spartanburg South Carolina
205.477.001015 Boehringer Ingelheim Investigational Site Union South Carolina
205.477.001013 Boehringer Ingelheim Investigational Site Nashville Tennessee
205.477.001022 Boehringer Ingelheim Investigational Site Corsicana Texas
205.477.001055 Boehringer Ingelheim Investigational Site Fort Worth Texas
205.477.001054 Boehringer Ingelheim Investigational Site Katy Texas
205.477.001062 Boehringer Ingelheim Investigational Site Tyler Texas
205.477.001030 Boehringer Ingelheim Investigational Site Abingdon Virginia
205.477.001008 Boehringer Ingelheim Investigational Site Roanoke Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01663987, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 16, 2018 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01663987 live on ClinicalTrials.gov.

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