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Not yet recruiting NCT07180888

Study of Diastolic Dysfunction in ESKD in Hemodialysis Patient

— Observational Heart Failure ESKD Hemodialysis Patients

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Echocardiography, Echocardiographic assessment of diastolic dysfunction.
Who it may be relevant to
Registry conditions: Heart Failure, ESKD, Hemodialysis Patients. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Overview

To Asses the prevalence , pattern , and severity of diastolic dysfunction in patients ESKD undergoing regular dialysis and to investigate its correlation with clinical parameters dialysis-related factors and echocardiographic findings

Interventions

  • Diagnostic test Echocardiography
    diastolic dysfunction in ESKD in hemodialysis by echocardiography
  • Diagnostic test Echocardiographic assessment of diastolic dysfunction
    non invasive transthoracic echocardiography including doppler and tissue doppler imaging will be used to assess left ventricular diastolic dysfunction parameters in hemodialysis patient

Primary outcome measures

  • diastolic dysfunction in ESKD in hemodialysis patient [Time frame: 4 months]

Eligibility criteria

Inclusion criteria

  • age between 18 and 65 years not diagnosed by MI able and willing to provide informed consent

Exclusion criteria

previous MI arrythmia CHF

\-

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07180888 · soh-med-25-7-21MS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗