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NCT03182309 Clinical Trial

Registry for Chronic Obstructive Pulmonary Disease With Sleep Apnea Hypopnea Syndrome in China

COPD Clinical Trial

Official title:
The Prevalence, Disease Course, Prognosis and Interaction of Chronic Obstructive Pulmonary Disease With Sleep Apnea Hypopnea Syndrome

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03182309
Other study ID # 2016YFC1304403
Secondary ID
Status Recruiting
Phase N/A
First received June 7, 2017
Last updated June 7, 2017
Start date June 15, 2017
Est. completion date December 31, 2020

Study information
Verified date June 2017
Source Chinese Academy of Medical Sciences, Fuwai Hospital
Contact Ke Hu, MD
Phone 18971035988
Email hukejx@163.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

COPD and sleep apnea dyspnea syndrome represent two of the most common chronic lung diseases. It is reported that the prevalence of COPD with sleep apnea dyspnea syndrome is also very high. COPD and sleep apnea may have pathological or genetics interactions so that patients having both disorders tend to have worse outcomes than either condition alone. Data reflecting the prevalence, disease course and outcome of overlap syndrome is very limited in China. Therefore, the aim of the study is to describe the prevalence, treatment and outcome in Chinese patients and exploring the underlying interaction mechanism.

Recruitment information / eligibility
Status Recruiting
Enrollment 3502
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria:

- COPD patients with informed consent

Exclusion Criteria:

- pregnant patients, patients with serious respiratory diseases other than COPD, patients with limited life expectancy, patients that can't coordinate well

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
China Renmin Hospital of Wuhan University Wuhan Hubei

Sponsors (1)
Lead Sponsor Collaborator
Chinese Academy of Medical Sciences, Fuwai Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary COPD acute exacerbation record the exacerbation events and related hospitalizations 3 years
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