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NCT03893409 Clinical Trial

GIRH Chronic Obstructive Pulmonary Disease Observational Study

Chronic Obstructive Pulmonary Disease Clinical Trial

Official title:
A Observational Study in Chinese Patients With Chronic Obstructive Pulmonary Disease (COPD)

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03893409
Other study ID # Respiratory disease of GIRH
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 10, 2018
Est. completion date December 30, 2022

Study information
Verified date March 2019
Source The First Affiliated Hospital of Guangzhou Medical University
Contact zhang zili, PHD
Phone 18922269968
Email zhangzili_04@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to establish the large COPD cohort and biological database in China, aiming for precision medicine to optimize diagnosis and treatment choices.

Recruitment information / eligibility
Status Recruiting
Enrollment 10000
Est. completion date December 30, 2022
Est. primary completion date December 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria:

-Aged 40-70 years COPD group: baseline post-bronchodilator FEV1/FVC < 0.7 Signed informed consent obtained prior to participations with the ability to comply with protocol and be available for study visits over 5 years

Exclusion Criteria:

- Acute exacerbation in the past 3 months Having other respiratory diseases with massive lung tissue destruction such as severe bronchiectasis and tuberculosis, etc The usual criteria of serious uncontrolled diseases thoracic or abdominal surgery in the last 3 months eye surgery in the last three months retinal detachment myocardial infarction in the last 3 months admission to hospital for any cardiac condition in the last month heart rate over 120 beats per minute antibacterial chemotherapy for tuberculosis pregnant or breast feeding

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
China The First Affiliated Hospital of Guangzhou Medical University Guangzhou Guangdong

Sponsors (1)
Lead Sponsor Collaborator
zili zhang

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary difference of FEV1 at 12 months from baseline difference of FEV1 at 12 months from baseline at 12 months
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