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Strain X Cardiopulmonary Test

Analysis Of Strain Myocardial Associated With The Exercise Tolerance In Patients With Heart Failure Systolic

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02869178
Enrollment
26
Registered
2016-08-16
Start date
2016-08-31
Completion date
Unknown
Last updated
2016-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Brief summary

Introduction : Patients with heart failure (HF ) with systolic dysfunction of moderate to severe exhibit significant reduction in the ability to exercise compared to those with mild dysfunction , and have worse prognosis. However, some clinical markers of severity and diagnosis widely used in this population such as ejection fraction (EF) , are not always able to translate the actual degree of cardiac damage as well as their relationship with the cardiorespiratory fitness of these individuals and prognosis . Objective: To evaluate the ability of the global longitudinal strain ( GLS ) in predicting exercise tolerance in heart failure patients with moderate and significant systolic dysfunction.

Interventions

None listed

Sponsors

Daniella Cunha Brandao
Lead SponsorOTHER

Study design

Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
21 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* moderate and significant systolic dysfunction (LVEF \< 45%) assessed by transthoracic echocardiography recent ( last month before evaluation ) Teichholz method , or when in the presence of contractile deficit target , by the Simpson method.

Exclusion criteria

* deformity in the face to prevent the coupling of the mask to perform the CPET , * orthopedic and neurological diseases that could make it impossible to perform the tests , * patients with psychiatric disorders that restricted them to respond to the questionnaire , * HF FC IV or hospitalization in the last three months , * angina unstable; * myocardial infarction or heart surgery up to three months before the survey ; * FEV1 / FVC \<70 % predicted characterizing obstructive respiratory disorder .

Design outcomes

Primary

MeasureTime frameDescription
Echocardiography for obtaining the strain 1 dayTo strain of technical analysis will be used echocardiography analysis software ( EchoPAC , GE Medical Systems, Horten , Norway, version 10.0 ) . The images will be analyzed in the longitudinal sections ( 4 bedrooms , 3 bedrooms and 2 cameras) . The endocardium is drawn manually from the septum to the lateral mitral annulus. A region of interest will be applied automatically by the software.

Secondary

MeasureTime frameDescription
Cardiopulmonary Test1 dayCardiopulmonary exercise testing will be carried out by the treadmill ramp method ( Centurium 300 , Micromed , Brazil ) through ErgoPC Elite® software associated with the electrocardiogram ( Micromed , Brazil ) with 12 channels. Respiratory variables will be evaluated by a gas analyzer ( Cortex - Metalyzer II , Germany) being obtained in standard conditions of temperature , pressure and humidity ( STPD ) , breath - by - breath , with the patient breathing in a face mask without leaks during exercise. Will be assessed during the test , functional capacity , measured in METs , VO2 , VE / VCO 2 , VE / VCO 2 slope , T1 / 2VO2 and RFC1 .

Countries

Brazil

Contacts

Primary ContactDaniella C Brandão, pHD
daniellacunha@hotmail.com+558121268000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026