CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,737 enrolled
Drug / intervention
Spiolto Respimatdrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02675517
NCT02675517N/ACompleted

Assessment of Physical Functioning and Handling of Spiolto® Respimat® in Patients With Chronic Obstructive Pulmonary Disease (COPD) Requiring Long-acting Dual Bronchodilation in Routine Clinical Practice

Boehringer Ingelheim·observational·Posted Feb 5, 2016·Updated Oct 15, 2018

In Brief

An observational study evaluating Spiolto Respimat for Pulmonary Disease, Chronic Obstructive. Completed, enrolled 1,737 participants across 1 site.

Detailed Summary

The primary objective of the study is to measure changes in physical functioning - serving as a surrogate for physical activity and exercise capacity - in COPD patients being treated with Spiolto® Respimat® after approximately 6 weeks. A secondary objective is to evaluate the patient¿s general condition (physician¿s evaluation) at visit 1 (baseline visit at the start of the study) and at visit 2 (final visit at the end of the study, approx. 6 weeks after visit 1), as well as patient satisfaction with Spiolto® Respimat® at visit 2.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesGermany
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 5, 2016
Enrollment StartJan 13, 2016
Primary CompletionMar 10, 2017
Study CompletionApr 11, 2017
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 10.4 years ago

Interventions

Spiolto Respimatdrug

Tiotropium bromide + Olodaterol