- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07579325
Lipid Screening Study
May 6, 2026 updated by: University of Central Florida
Prospective Screening for Elevated Lipoprotein(a) in an Adult Primary Care Population
The purpose of this pilot study is to estimate the prevalence of elevated Lipoprotein (a) in an adult primary care population and to describe the distribution of atherogenic lipid markers within this cohort.
This pilot study will provide preliminary data to inform future cardiovascular risk assessment initiatives in primary care.
Study Overview
Study Type
Observational
Enrollment (Estimated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Britney-Ann Wray, BS, CTBS, CCRP
- Phone Number: 4072668742
- Email: britney-ann.wray@ucf.edu
Study Contact Backup
- Name: Amoy Fraser, PhD, CCRP, PMP
- Phone Number: 14072668742
- Email: Amoy.Fraser@UCF.edu
Study Locations
-
-
Florida
-
Orlando, Florida, United States, 32827
- Recruiting
- University of Central Florida
-
Contact:
- Amoy Fraser, PhD, CCRP, PMP
- Phone Number: 4072668742
- Email: Amoy.Fraser@UCF.edu
-
Contact:
- Britney-Ann Wray, BS, CTBS, CCRP
- Phone Number: 4072668742
- Email: britney-ann.wray@ucf.edu
-
Principal Investigator:
- Stephanie Perez, MSN, MBA, ARNP, CLS, BHCN
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
As any adult patient can be enrolled, no pre-screening will be done.
UCFH only sees adult patients.
Description
Inclusion Criteria:
- Adults aged 18 years or older
- Receiving care at UCF Health primary care clinic
- Able to understand and provide informed consent and HIPAA authorization
Exclusion Criteria:
- Patient self discloses any medical condition that would make venipuncture unsafe
- Pregnant women
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lipoprotein(a) prevalence in Adults
Time Frame: 3 months
|
The purpose of this pilot study is to estimate the prevalence of elevated Lipoprotein (a) in an adult primary care population and to describe the distribution of atherogenic lipid markers within this cohort.
This pilot study will provide preliminary data to inform future cardiovascular risk assessment initiatives in primary care.
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Stephanie Perez, MSN, MBA, ARNP, CLS, BHCN, University of Central Florida
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 5, 2026
Primary Completion (Estimated)
July 1, 2026
Study Completion (Estimated)
August 1, 2026
Study Registration Dates
First Submitted
May 6, 2026
First Submitted That Met QC Criteria
May 6, 2026
First Posted (Actual)
May 12, 2026
Study Record Updates
Last Update Posted (Actual)
May 12, 2026
Last Update Submitted That Met QC Criteria
May 6, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY0009025
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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