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NCT07197242Not yet recruiting

Prognostic Role of Lipoprotein(a) in Elective Percutaneous Coronary Revascularization

Assessment of Lipoprotein(a) in Patients Undergoing Elective Percutaneous Coronary Revascularization: Implications for Cardiovascular Risk Stratification

Source: ClinicalTrials.gov · Last updated 29 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The study investigates the role of Lipoprotein(a) \[Lp(a)\] levels in predicting cardiovascular risk and adverse events in patients undergoing elective percutaneous coronary intervention (PCI).

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
156 (estimated)
First submitted
20 Sept 2025
Start date
1 Oct 2026
Primary completion date
30 Jun 2027
Lead sponsor
Assiut University
NCT number
NCT07197242

What you commit to

  • Study type: Observational
  • Planned participants: 156
  • From 1 Oct 2026 to the primary completion date, 30 Jun 2027
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Acute coronary syndrome within 30 days
    • Cardiogenic shock
    • Prior heart transplant or left ventricular assist device (LVAD)
    • Life expectancy less than 1 year due to non-cardiac causes
    • Participation in a blinded Lp(a)-lowering outcome trial at the time of enrollment

Who the study is looking for

  • Adults aged 18 years or older
    • Undergoing elective PCI for stable coronary artery disease
    • Ability to provide informed consent
    • Willingness to undergo blood sampling prior to PCI

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.