Clinical trial
A Double-blind, Placebo Controlled Trial to Assess the Safety of Two-week Administration of 80 mcg q.i.d. and 160 mcg q.i.d. of Ipratropium Bromide, as Delivered by the RESPIMAT® Device, in Patients With Chronic Obstructive Pulmonary Disease
NCT02236182 is registered in ClinicalTrials.gov with Boehringer Ingelheim as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Double-blind, Placebo Controlled Trial to Assess the Safety of Two-week Administration of 80 mcg q.i.d. and 160 mcg q.i.d. of Ipratropium Bromide, as Delivered by the RESPIMAT® Device, in Patients With Chronic Obstructive Pulmonary Disease
- Lead sponsor
- Boehringer Ingelheim
- Phase
- Phase 2
- Overall status
- Completed
- Start date
- July 31, 1998
- Completion date
- Not reported
- Enrollment
- 57 (actual)
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.