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Recruiting NCT06779513

Validation and Assessment of Novel Morphology-Voltage-P-wave Score for Diagnosing Left Ventricular Diastolic Dysfunction in Patients With Hypertension

Observational Hypertension

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: Echocardiohraphy.
Who it may be relevant to
Registry conditions: Hypertension. Basic parameters: 18 years — 70 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
Indonesia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study aimed to assess and validate the diagnostic utility of a novel Morphology-Voltage-P-wave Score (MVP Score) in identifying left ventricular diastolic dysfunction among patients with hypertension. Researchers will collect information of patient with hypertension and underwent transthoracal echocardiography assessment. The data consist of demographic data, clinical presentation, laboratory, and echocardiography result were collected by two investigators. Then, the data was analyzed by using IBM SPSS Statistics v26.

Interventions

  • Diagnostic test Echocardiohraphy
    Transthoracal echocardiography for diastolic function assessment

Primary outcome measures

  • Diastolic Dysfunction [Time frame: Up to 1 weeks]

Eligibility criteria

Inclusion criteria

  • Essential hypertension

Exclusion criteria

  • Secondary or resistant hypertension
  • LVEF<55%
  • Congenital heart disease
  • Infiltrative cardiomyopathy
  • Coronary artery disease
  • Chronic kidney disease
  • Valvular heart disease
  • Bundle branch block
  • Arrhythmia

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

Healthy volunteers: No

Study design

Observational model
Case-control

Study locations

Indonesia · 1 center
  • Dr. Kariadi Central General Hospital — Semarang

Identifiers

NCT: NCT06779513 · Undip_Kardio 4

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗