A Study to Evaluate the Symptoms over 24 hours in Patients with Chronic Obstructive Pulmonary Disease - LASSYC Study - LASSYC

Study identifier:D2287R00119

ClinicalTrials.gov identifier:NCT03381560

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

An observational, cross-sectional study of primary data collection to describe symptoms over 24 hours and their relationship with adherence to respiratory treatment, direct costs and PRO in stable COPD patients in Brazil.

Medical condition

Chronic Obstructive Pulmonary Disease

Phase

-

Healthy volunteers

No

Study drug

-

Sex

All

Actual Enrollment

602

Study type

Observational

Age

40 Years - 130 Years

Date

Study Start Date: 07 Nov 2017
Primary Completion Date: 30 Jun 2018
Study Completion Date: 30 Jun 2018

Study design

Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Jun 2019 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria