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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03187236
Other study ID # 2016YFC1304404A
Secondary ID
Status Recruiting
Phase N/A
First received June 13, 2017
Last updated June 13, 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 Jiangna Han, MD
Phone 13520053104
Email 13520053104@139.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Anxiety and depression are common comorbidities of chronic obstructive pulmonary disease (COPD). However, the exact prevalence is not known in China. COPD patients with anxiety and depression tend to have more severe symptoms and worse prognosis, but the related evidences are not strong enough. The study aim to investigate the prevalence and long-term outcome of anxiety and depression in COPD.


Recruitment information / eligibility

Status Recruiting
Enrollment 1906
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers
Gender All
Age group N/A to 80 Years
Eligibility Inclusion Criteria:

- Stable chronic obstructive pulmonary disease (COPD) patients

Exclusion Criteria:

- Patients with bronchial asthma or other severe pulmonary diseases or having received pulmonary surgery in 6 months

- Patients with tumor history during past 5 years

- Patients with COPD exacerbations during past 4 weeks

- Participants in clinical trials

- Patients in pregnancy or breastfeeding

- Patients unable to complete questionaire independently

- Patients older than 80 years old

- Patients receiving long-term domiciliary oxygen therapy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Peking Union Medical College Hospital Beijing Beijing

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 moderate and severe COPD exacerbations total times 3 years
Secondary All-cause mortality mortality in % 3 years
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