Clinical trial Recruiting at 1 site Observational Ages 18 to 100

Using Fetuin A to Predict Kidney Function Decline in Patients with High Blood Pressure

Official title: Modified Urine Fetuin A as a Predictor of Deterioration of Renal Function in Patients With Resistant and Non-resistant Hypertension

Run by University Hospital Ostrava · NCT05963126 · Data updated 2026-11-12

This study is testing if a substance in urine called Fetuin A can help predict kidney problems in people with high blood pressure.

Quick facts

Study typeObservational
Ages18 Years to 100 Years
SexAll
Enrollment200 (estimated)
SponsorUniversity Hospital Ostrava
Academic / other
Locations1 site (Ostrava, Czech Republic)
StatusRecruiting
StartedJuly 1, 2023
Main results expectedDecember 31, 2025
Study endsDecember 31, 2026
Registry record updatedJuly 27, 2023
Trial IDNCT05963126 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients with arterial hypertension who are being treated with at least one antihypertensive agent.

Probably not a fit

Patients with diabetes mellitus, severe hypertension, or those undergoing renal replacement therapy will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to evaluate the potential of modified human urine Fetuin A as an early biomarker for predicting the deterioration of renal function in patients with arterial hypertension. Current methods for assessing kidney function often fail to detect early impairment, particularly in patients with diabetes who do not show microalbuminuria. By focusing on hypertonic patients, this study seeks to fill a gap in existing research regarding the predictive capabilities of urine Fetuin A. The study will involve monitoring patients treated for arterial hypertension without any interventions.

Why it matters

Potential benefit: If successful, this study could lead to earlier detection of kidney disease in patients with high blood pressure, allowing for timely interventions.

How similar studies have gone: While studies on urine Fetuin A in other contexts exist, this specific approach in hypertonic patients is novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Arterial hypertension treated by at least one antihypertensive agent

Exclusion Criteria:

* Diabetes mellitus of any type, defined as fasting glucose \>7,0 mmol/l or any glycemia \>11,0 mmol/l, or HbA1c\>48 mmol/mol
* Decompensated arterial hypertension defined as office blood pressure \>180/110 mmHg or on Ambulatory Blood Pressure Monitoring (ABPM)
* Patient with renal replacement therapy
* Present rheumatoid disease (rheumatoid arthritis, systemic lupus, sclerodermia, dermatomyositis, Inflammatory Bowel Disease, etc.), positivity of antinuclear antibody (ANA) / extractable nuclear antigen (ENA) screening
* Acute infection defined as C-Reactive Protein (CRP) \>50 mg/l
* Severe impairment of liver function defined as cirrhosis, Alanine Transaminase or ASpartate Transferase (ALT or AST) \>10 µkat/l
* Terminal incurable illness

Where it's running

  • University Hospital Ostrava, - Department of Internal Medicine and Cardiology
    Ostrava, Czech Republic, Czechia
    Recruiting

Study contacts

  • Principal investigator: Zdeněk Ramík, MD — University Hospital Ostrava
  • Study coordinator: Jiří Hynčica
  • Email: jiri.hyncica@fno.cz
  • Phone: 0042059737

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.