HFpEF and 2-year Mortality of COPD Patients

NCT ID: NCT04277429

Last Updated: 2022-11-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-07-01

Study Completion Date

2025-04-01

Brief Summary

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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

Detailed Description

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Conditions

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Chronic Obstructive Pulmonary Disease Heart Failure

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Normal cardiac function

Normal cardiac function

Cardiac function assessment

Intervention Type DIAGNOSTIC_TEST

Echocardiography, cardiac enzymes analysis

Heart failure with reduced ejection fraction

Heart failure with reduced ejection fraction

Cardiac function assessment

Intervention Type DIAGNOSTIC_TEST

Echocardiography, cardiac enzymes analysis

Heart failure with preserved ejection fraction

Heart failure with preserved ejection fraction

Cardiac function assessment

Intervention Type DIAGNOSTIC_TEST

Echocardiography, cardiac enzymes analysis

Interventions

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Cardiac function assessment

Echocardiography, cardiac enzymes analysis

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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
Minimum Eligible Age

40 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital Olomouc

OTHER

Sponsor Role lead

Responsible Party

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Milan Sova

Principal Investigator, Department of Respiratory Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Milan Sova, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Department of Respiratory Medicine

Locations

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Frydek Mistek Hospital

Frýdek-Místek, , Czechia

Site Status NOT_YET_RECRUITING

University Hospital Olomou

Olomouc, , Czechia

Site Status RECRUITING

Countries

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Czechia

Central Contacts

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Milan Sova, Ph.D.

Role: CONTACT

588445326

Ondrej Zela, MD

Role: CONTACT

Facility Contacts

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Ondrej Zela

Role: primary

Milan Sova

Role: primary

588445326

Other Identifiers

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THERESE

Identifier Type: -

Identifier Source: org_study_id

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