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NCT04277429 Clinical Trial

HFpEF and 2-year Mortality of COPD Patients

Heart Failure Clinical Trial

— THERESE  

Official title:
The Influence of hearT Failure With Preserved Ejection Fraction on 2year Mortality of Patients With cHronic obstructivE pulmonaRy disEaSE- THERESE Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04277429
Other study ID # THERESE
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2020
Est. completion date April 1, 2025

Study information
Verified date November 2022
Source University Hospital Olomouc
Contact Milan Sova, Ph.D.
Phone 588445326
Email milan.sova@email.cz
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study was designed to assess potential relationship between heart failure with preserved ejection fraction and 2- year mortality of patients with chronic obstructive pulmonary disease

Recruitment information / eligibility
Status Recruiting
Enrollment 150
Est. completion date April 1, 2025
Est. primary completion date April 1, 2025
Accepts healthy volunteers No
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria: Exacerbation of chronic obstructive pulmonary disease requiring hospitalization Age 40 - 80 years Performance status 0-1 according to Eastern Cooperative Oncology Group (ECOG) Long acting beta agonist (LABA)/ long acting antimuscarinic (LAMA) bronchodilator treatment Exclusion Criteria: Presence of major heart valve dysfunction Documented noncompliance with treatment Presence of active malignancy Body mass index > 40 Interstitial lung disease

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Cardiac function assessment
Echocardiography, cardiac enzymes analysis

Locations
Country Name City State
Czechia Frydek Mistek Hospital Frýdek-Místek
Czechia University Hospital Olomou Olomouc

Sponsors (1)
Lead Sponsor Collaborator
University Hospital Olomouc

Country where clinical trial is conducted

Czechia, 

Outcome
Type Measure Description Time frame Safety issue
Primary Mortality Mortality of patients 2 year
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