Urinary Proteomics Combined With Home Blood Pressure Telemonitoring for Health Care Reform
Launched by KU LEUVEN · Mar 5, 2020
Trial Information
Current as of July 25, 2025
Not yet recruiting
Keywords
ClinConnect Summary
The UPRIGHT-HTM trial is studying a new way to monitor and treat patients with health conditions related to high blood pressure and protein levels in urine. Researchers want to see if combining home blood pressure monitoring with a special urine test can help identify patients at higher risk for health problems more effectively than just monitoring blood pressure alone. This could lead to better treatment plans and potentially reduce healthcare costs, while also empowering patients to take an active role in managing their health.
To participate in this study, you would need to have at least three risk factors for heart problems, like high blood pressure or type 2 diabetes. You'll also need to be comfortable taking your blood pressure at home every day and have access to the internet through a device like a smartphone or computer. If you join the study, you can expect to follow a specific plan for monitoring your health over time. However, there are some exclusions, like having type 1 diabetes or certain serious illnesses, so it's best to check if you meet the criteria before considering participation.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients must have at least three additional guideline-defined risk factors, preferably including hypertension, type 2 diabetes mellitus (T2DM), or both;
- • Patients should be willing patients to engage for the duration of the study in home blood pressure telemonitoring (1 reading per day);
- • Patients must have an email address and internet access via smartphone, tablet, or laptop or desktop computer;
- • Patients should comply with the study protocol during the run-in phase.
- Exclusion Criteria:
- • Type 1 diabetes mellitus;
- • Absence of a practicable echocardiographic window;
- • Previous or concurrent severe cardiovascular or non-cardiovascular disease;
- • Cancer within 5 years of enrolment;
- • Suspected substance abuse;
- • Psychiatric illness;
- • Use of nephrotoxic drugs;
- • Particpation in another clinical study.
About Ku Leuven
KU Leuven, a prestigious research university located in Belgium, is renowned for its commitment to advancing medical science and improving patient care through innovative clinical trials. With a strong emphasis on interdisciplinary collaboration, KU Leuven integrates cutting-edge research with clinical practice, facilitating the development of new therapeutic strategies and medical technologies. The institution's robust infrastructure and expertise in various fields, including biotechnology, pharmacology, and public health, position it as a leader in conducting high-quality clinical research that adheres to rigorous ethical standards and regulatory requirements. Through its clinical trials, KU Leuven aims to contribute significantly to the global biomedical landscape and enhance health outcomes for diverse populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Gentofte, , Denmark
Brussels, , Belgium
Gent, , Belgium
Mechelen, , Belgium
Hannover, , Germany
Athens, , Greece
Abuja, , Nigeria
Gdańsk, , Poland
Kraków, , Poland
Ljubljana, , Slovenia
Potchefstroom, , South Africa
Montevideo, , Uruguay
Patients applied
Trial Officials
Lutgarde Thijs, MSc
Principal Investigator
University of Leuven
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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