Home › Lipid Metabolism Disorders › NCT05693701
Multicomponent Intervention Study- Blood Donors With High Cholesterol
Recruiting
Implementing a Multicomponent Intervention to Treat Blood Donors With Familial Hypercholesterolemia
Who can join
Ages 18 to 75 · All sexes
Full eligibility criteria
Inclusion Criteria: * Blood donors from Carter BloodCare with high cholesterol meeting MEDPED FH criteria * Age 18 to 75 years Exclusion Criteria: * Currently taking medication to lower cholesterol * Taking any medication that can interact with statins * Pregnancy * Identified secondary cause of elevated lipids * Chronic liver disease or significantly elevated liver function tests (\> 3 times upper limit)
About the study
The purpose and objective of this study is to improve cholesterol treatment among blood donors with FH (Familial Hypercholesterolemia).
What is being tested
- Implementation Strategy Bundle (behavioral)
- Usual care notification (other)
Sponsor: University of Texas Southwestern Medical Center · Participants: 100 · Started: Feb 27, 2023
Contact the study team
- Amit Khera, MD · Phone: 214.645.7500
- Lakeisha Cade · Phone: 214.648.2878
Official record on ClinicalTrials.gov — NCT05693701
Locations in the U.S.
| Texas | UT Southwestern Medical Center, Dallas |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.