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NCT Number: NCT06413160

The Cardiovascular-Renal-Metabolic (CRM) Syndrome Survey in Jordan

Cardiovascular-renal-metabolic (CRM) syndrome is defined as a systemic disorder with a collection of related signs and symptoms attributable to the coexistence of multiple cardiovascular, renal and metabolic disease with a common underlying pathophysiology in one individual. Surveying this syndrome in a large population in Jordan aims at studying the risk factors, components and stages of the syndrome, thus helping early screening, diagnosing and treating disease and its risk factors.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

Cardiovascular-renal-metabolic (CRM) syndrome is defined as a systemic disorder with a collection of related signs and symptoms attributable to the coexistence of multiple cardiovascular, renal and metabolic disease with a common underlying pathophysiology in one individual.

CRM syndrome reflects the intersection of cardiovascular disease with chronic kidney disease (CKD), and metabolic disease and risk factors (RF). A critical combination of these diseases and their risk factors in the same individual has a profound impact on quality of life and overall mortality. The clinical implications of the presence of CRM are significant, with premature morbidity and mortality, multiple organ-system disease, and high health care budgets mainly driven by the burden of cardiovascular disease (CVD).

There are high prevalence rates of all components of CRM and its RF on a global level and in the Middle East. Of note is the high prevalence of CV in the young, smoking, diabetes mellitus, obesity and dyslipidemia.

The current study will evaluate the prevalence of components and RF of CRM disease in a large population in North, central and South of Jordan.

In the Middle East, no systematic study has evaluated the definition of CRM, definition of its stages, and prevalence of its RF and its relation to the coexisting social determinants of health.

The study will provide new and contemporary knowledge on the definition, staging, and comprehensive approaches to care for patients with CRM, and subsequently exploring opportunities for prevention and care optimization by life style modification and pharmacotherapy.

There are different aspects that explain the interaction between the components of CRM. (A) The bidirectional association between the heart failure and the kidneys (cardiorenal syndrome) in addition to the risk of CAD in patients with CKD, (B) adipose tissue link to atherosclerosis mediated by inflammation, insulin resistance and endothelial dysfunction, and risk for DM (C) DM link to CVD, heart failure and kidney dysfunction., and many other links as well.

Screening for CRM is an important pillar in promoting health in every community. The CRM staging system facilitates identifying individuals at progressive levels of severity starting from the preclinical phase to delay or avoid the onset of clinical CVD and CKD. To appropriately find individuals at stage 0 (i.e., asymptomatic stage) it is important to undertake active screening within the population.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults (age 18 years and above).
  • Willing to sign an informed consent.

Exclusion criteria

  • None.

Treatment and study plan

Primary outcomes

  1. Prevalence of cardiovascular-renal-metabolic syndrome

    Time frame: From date of study entry through study completion, an average of 1 year

    • CVD A. Coronary heart disease: Silent and clinical CAD (chronic stable coronary disease, acute coronary disease [ST-elevation myocardial infarction and non-ST-elevation acute coronary syndrome].

    B. Heart failure. C. Atrial fibrillation. D. Stroke. E. Peripheral artery disease

    • Renal: chronic kidney disease
    • Metabolic:

    A. Obesity/ B. Diabetes mellitus (DM).

Secondary outcomes

  1. Elevated levels of blood markers

    Time frame: From date of study entry through study completion, an average of 1 year

    Elevated level of lipoprotein (a) , homocysteine, high sensitivity C-Reactive Protein, insulin resistance, and Urine Creatinine/Albumin ratio.

Study contacts

Contact information is provided by the study sponsor or research team.

Ayman Hammoudeh, MD, FACC

CONTACT

[email protected]

065001000

Imad A Alhaddad, MD, FACC

CONTACT

[email protected]

065608080

Sponsors and collaborators

Lead sponsor

Jordan Collaborating Cardiology Group

Other

Collaborators

  • Cardiovascular Academy
  • The Association of Jordanian Medical Laboratory Specialists AJMLS

Registry information

Acronym: JoCRMSSurvey

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
May 14, 2024
Registry last updated
Dec 30, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.