Registry of patients with high lipoprotein(a) levels

The Prevalence, Patients' Characteristics, and Hyper-Lp(a)-Emia Risk Factors in the Polish Population. The Polish Mother's Memorial Hospital Research Institute Lipoprotein(a) Registry

Observational Polish Mother Memorial Hospital Research Institute · NCT06610669

This study is collecting information from patients with high lipoprotein(a) levels to better understand how it affects their health and what other conditions they might have.

Quick facts

Study typeObservational
Enrollment2000 (estimated)
SexAll
SponsorPolish Mother Memorial Hospital Research Institute Academic / other
Locations1 site (Lodz)
Trial IDNCT06610669 on ClinicalTrials.gov

What this trial studies

The PMMHRI-Lp(a)-Registry is a non-interventional, observational registry that collects data on patients with measured lipoprotein(a) concentrations at the Polish Mother's Memorial Hospital Research Institute. Established in January 2022, it includes patients from the Departments of Cardiology and Endocrinology, focusing on those with elevated Lp(a) levels as per the latest Polish guidelines. The registry gathers comprehensive patient information, including demographics, comorbidities, medications, and cardiovascular risk scores, to better understand the prevalence and implications of hyper-Lp(a)-emia.

Who should consider this trial

Good fit: Ideal candidates for this registry are patients who have had their lipoprotein(a) levels measured and are receiving care in the relevant departments.

Not a fit: Patients who have not had their lipoprotein(a) levels measured or do not have relevant cardiovascular or endocrine conditions may not benefit from this registry.

Why it matters

Potential benefit: If successful, this registry could enhance understanding of hyper-Lp(a)-emia and improve management strategies for affected patients.

How similar studies have performed: While this registry approach is not novel, it builds on existing knowledge and practices in the field of lipid management, potentially contributing valuable data to ongoing discussions about hyper-Lp(a)-emia.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* measured lipoprotein(a) concentration

Exclusion Criteria:

\-

Where this trial is running

Lodz

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Lipoprotein, Hyper-Lp-Emialipoprotein
Last reviewed 2026-06-10 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.