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Search / Trial NCT04299529

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.

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

0 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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