ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Efficacy and Safety of 2 Doses of Tiotropium Respimat® Compared to Placebo in Children With Severe Persistent Asthma

ClinicalTrials.gov ID: NCT01634152

Public ClinicalTrials.gov record NCT01634152. 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 May 20, 2026, 10:24 AM 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 Randomised, Double-blind, Placebo-controlled, Parallel-group Trial to Evaluate Efficacy and Safety of Tiotropium Inhalation Solution (2.5 mcg and 5 mcg) Delivered Via Respimat® Inhaler Once Daily in the Evening Over 12 Weeks as add-on Controller Therapy on Top of Usual Care in Children (6 to 11 Years Old) With Severe Persistent Asthma

Study identification

NCT ID
NCT01634152
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
401 participants

Conditions and interventions

Conditions

Interventions

  • Placebo Drug
  • Tiotropium high dose Drug
  • Tiotropium low dose mcg Drug

Drug

Eligibility (public fields only)

Age range
6 Years to 11 Years
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
Jun 30, 2012
Primary completion
Apr 30, 2015
Completion
Apr 30, 2015
Last update posted
Jan 28, 2016

2012 – 2015

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
205.446.01014 Boehringer Ingelheim Investigational Site Rolling Hills Estates California
205.446.01011 Boehringer Ingelheim Investigational Site Denver Colorado
205.446.01003 Boehringer Ingelheim Investigational Site North Dartmouth Massachusetts
205.446.01009 Boehringer Ingelheim Investigational Site Columbia Missouri
205.446.01005 Boehringer Ingelheim Investigational Site Cincinnati Ohio
205.446.01010 Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma
205.446.01004 Boehringer Ingelheim Investigational Site Charleston South Carolina
205.446.01002 Boehringer Ingelheim Investigational Site North Charleston South Carolina
205.446.01012 Boehringer Ingelheim Investigational Site Arlington Texas
205.446.01013 Boehringer Ingelheim Investigational Site San Antonio Texas

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 84 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01634152, 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 Jan 28, 2016 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01634152 live on ClinicalTrials.gov.

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