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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04123028
Other study ID # 60-319-14-3
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 1, 2017
Est. completion date December 31, 2018

Study information

Verified date October 2019
Source Prince of Songkla University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The association of blood eosinophil as a biomarker for eosinophilic Thai COPD patients, such as COPD exacerbation, hospital admission, lung functions and mortlity.


Description:

The prospective one year study in Thai COPD patients for the clinical outcomes of COPD compare between eosinophilic and non-eosinophilic which determine by blood eosinophil counts equal or more than 300 cells/microliters. The primary outcomes was COPD exacerbation, the secondary outcomes were lung function, dyspnea and quality of life.


Recruitment information / eligibility

Status Completed
Enrollment 145
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria:

- diagnosis of COPD by GOLD criteria

Exclusion Criteria:

1. high blood eosinophil from known causes such as systemic corticosteroid use, malignancy, parasitic infection

2. Patients who had previous acute exacerbation within 30-day before study entry

3. Patients who had previous systemic corticosteroids used within 30-day before study entry

Study Design


Related Conditions & MeSH terms


Intervention

Other:
observatory
observation for 1 year period

Locations

Country Name City State
Thailand Faculty of Medicine, Prince of Songkla university Songkhla

Sponsors (1)

Lead Sponsor Collaborator
Prince of Songkla University

Country where clinical trial is conducted

Thailand, 

References & Publications (1)

Bafadhel M, Pavord ID, Russell REK. Eosinophils in COPD: just another biomarker? Lancet Respir Med. 2017 Sep;5(9):747-759. doi: 10.1016/S2213-2600(17)30217-5. Epub 2017 Jun 7. Review. Erratum in: Lancet Respir Med. 2017 Aug;5(8):e28. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Acute worsening of respiratory symptoms acute severe worsening of respiratory symptoms 1 year
Secondary Physiological outcomes Forced expiratory volume in one second 1 year
Secondary health related quality of life Chronic Obstructive Pulmonary Disease Assessment Test (CAT) scores which the minimum 0 and maximum 40 values, and whether higher scores mean a worse outcome. 1 year
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