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Pulse Wave Analysis and Velocity in Patients With Chronic Renal Failure: a Cross-sectional Observational Study to Assess Association With Left Ventricular Hypertrophy, Uremic Toxins and Inflammation.

U

Universitaire Ziekenhuizen KU Leuven

Status

Completed

Conditions

CHRONIC RENAL FAILURE
Left Ventricular Hypertrophy
Arterial Stiffness

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The aims of the presented study are as follows:

  1. To evaluate the endothelial function and arterial stiffness in a large cohort of prevalent CKD patients by means of non-invasive applantion tonometry.
  2. To evaluate the association between the serum levels of the representatives of the various classes of uremic toxins and markers of endothelial function and arterial stiffness.
  3. To evaluate the association between markers of inflammation and oxidative stress and markers of endothelial function and arterial stiffness.
  4. To evaluate the association between echocardiographic parameters and markers of arterial stiffness

Enrollment

90 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age: 18-60
  • Chronic kidney disease: according to the K-DOQI guidelines ( kidney damage ≥ three months, as defined by structural or functional abnormalities of the kidney, with or without decreased GFR, manifest by either: pathological abnormalities; or markers of kidney damage, including damage in the composition of blood or urine test, or abnormalities in imaging tests; GFR< 60 ml/min/1.73m² for ≥ three months, with or without kidney damage)
  • Written informed consent

Exclusion criteria

  • major illnesses( life expectancy of < 1 year)
  • history of atrial fibrillation
  • history of myocardial infarction, unstable angina, congestive heart failure, peripheral vascular diasease ,cerebrovascular disease, diabetes

(nonechogenic)

Trial design

90 participants in 1 patient group

CKD patients

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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