Integrating Whole Genome Sequencing and Digital Twins Into the Management of Hypercholesterolemia in Emiratis
Launched by ABU DHABI HEALTH SERVICES COMPANY · Jul 30, 2024
Trial Information
Current as of July 01, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new way to manage high cholesterol, known as hypercholesterolemia, in Emirati patients. Researchers are looking at how whole genome sequencing (which analyzes a person's complete DNA) and digital twin technology (a virtual model of a patient that helps predict health outcomes) can improve treatment strategies. The goal is to develop guidelines that can be used in larger studies later on and to help incorporate genetic information into everyday healthcare practices.
To be eligible for this study, participants must be Emirati adults aged 18 to 55 who have high levels of LDL cholesterol (often called "bad" cholesterol) in their blood. Specifically, they should have had two or more LDL-C readings above 190 mg/dL in the past year and should not have been on cholesterol-lowering medication for the last three months. Participants should be fluent in either English or Arabic. If you join the study, you will help researchers better understand how to treat high cholesterol in a way that is tailored to individual patients. It's important to note that certain health conditions or medications may disqualify someone from participating.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients with 2 or more LDL-C levels greater than 190 mg/dL or 5.0 mmol/L in the past 12 months
- • Undiagnosed patients meeting Possible, Probable or Definitive FH criteria according to Dutch Lipid Clinic Network (DLCN) criteria (Eur Heart J. 2011 Jul;32(14):1769-818. doi: 10.1093/eurheartj/ehr158. Epub 2011 Jun 28.)
- • Patients who have not been on anti-lipidemic medication in the past 3 months
- • Ages 18-55
- • Emirati national
- • All patients must be fluent in English or Arabic
- Exclusion Criteria:
- • - Patients who do not meet the above criteria
- • Patients with a previous diagnosis of FH
- • Patients with a progressive debilitating illness
- • Patient with untreated hypothyroidism, history of proteinuria, obstructive liver disease, chronic renal failure, human immunodeficiency virus infection, or on immunosuppressant or steroid or psychiatric medications
- • Patients with untreated clinical anxiety or depression (as measured by a Hospital Anxiety and Depression Scale (HADS) score of ≥ 16 on the depression subscale)
- • Patients who are pregnant
About Abu Dhabi Health Services Company
Abu Dhabi Health Services Company (SEHA) is a leading healthcare provider in the United Arab Emirates, committed to delivering high-quality medical services and advancing healthcare innovation. As a prominent sponsor of clinical trials, SEHA focuses on enhancing patient care through rigorous research and development initiatives. The organization collaborates with local and international partners to facilitate studies that address critical health challenges, ensuring adherence to the highest ethical and regulatory standards. By fostering an environment of scientific inquiry, SEHA aims to contribute to the global medical community and improve health outcomes for diverse populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Abu Dhabi, , United Arab Emirates
Patients applied
Trial Officials
Abdulmajeed BS Alzubaidi, MD
Principal Investigator
Abu Dhabi Health Services Co. -SEHA
Erik J Koornneef, PHD
Study Director
Abu Dhabi Health Services Co. -SEHA
Mhy-Lanie Adduru, MD
Study Director
Predictiv Care, Inc.
Salah Eldin HM Hu, MD
Study Chair
Abu Dhabi Health Services Co. -SEHA
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported