Lp(a) Screening
OtherParticipants will provide demographic information and have a blood draw for Lp(a) levels if they are unknown.
NCT Number: NCT05378529
The purpose of this study is to characterize the distribution of lipoprotein(a) (Lp(a)) levels among participants with a history of ASCVD as defined by their medical history and is 2-fold:
* Evaluate the distribution of Lp(a) value in the overall participants with documented history of ASCVD * Evaluate the distribution of Lp(a) value in participants with documented history of ASCVD by demographics and regions
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Notify Me18 year–85 year
All sexes
Interventional
Not applicable
Inst. de Inv. Clinicas Bahia Blanca, Bahía Blanca, Buenos Aires, Argentina
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will provide demographic information and have a blood draw for Lp(a) levels if they are unknown.
Time frame: Up to approximately 2 weeks
Time frame: Up to approximately 2 weeks
Blood sampling will be performed in cases where Lp(a) values are not available at enrollment. In cases where Lp(a) values are available, data will be collected retrospectively.
Time frame: Up to approximately 2 weeks
Amgen
Industry
A Multicenter, Cross-sectional Study to Characterize the Distribution of Lipoprotein(a) Levels Among Patients With Documented History of Atherosclerotic Cardiovascular Disease
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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.
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