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Evaluation of Endothelial Dysfunction in Geriatric Non-dialysis Chronic Kidney Disease Patients

Evaluation of Endothelial Dysfunction in Geriatric Non-dialysis Chronic Kidney Disease Patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07430982
Acronym
EDGeriatrCKD
Enrollment
101
Registered
2026-02-24
Start date
2023-05-12
Completion date
2026-02-01
Last updated
2026-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carotis Intima-media Thickness, Chronic Kidney Disease, Geriatrics

Keywords

geriatrics, chronic kidney disease, soluble vascular endothelial cadherin, FGF-23

Brief summary

Brief summary template The goal of this clinical trial is to assess endothelial dysfunction in geriatric non-dialysis CKD patients. The main questions it aims to answer are: • In geriatric non-dialysis CKD patients, the study aimed to demonstrate the relationship between soluble vascular endothelial cadherin and fibroblast growth factor-23 levels, which are indicators of endothelial dysfunction-and therefore a possible cardiovascular risk factor-using measurement methods such as ultrasonographic carotid intima-media thickness, flow-mediated dilation, and nailfold capillaroscopy. Participants will have measurement of; * ultrasonographic carotid intima-media thickness, * flow-mediated dilation, * nailfold capillaroscopy * venous blood sampling * Visit the clinic once,

Detailed description

In this single-center study, we aimed to evaluate endothelial dysfunction, the leading cause of mortality in geriatric CKD patients. We kept patient exclusion criteria strict and considered it more rational to conduct this study in a patient group requiring proactive intervention by excluding patients with 'known' cardiovascular disease. For this purpose, we used some non-invasive parameters known in the literature (ultrasonographic measurement of carotid intima-media thickness, nailfold capillaroscopy, flow-mediated dilation). We also planned to measure serum sVE Cadherin levels, which have not been clearly evaluated in geriatric CKD patients before, as well as serum FGF23 levels. We also planned to evaluate the relationship and correlation of these different parameters with other standard biochemical and anthropometric measurements. Patient recruitment for the study took place between May 12, 2023, and September 11, 2023. We followed up for mortality for approximately 2.3 years.

Interventions

DIAGNOSTIC_TESTUltrasonographic and Capillary Measurements

All measurements will be applied to the entire patient group.

Sponsors

Muğla Sıtkı Koçman University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with CKD who are not receiving RRT and those aged 65 and over

Exclusion criteria

* Patients under 65 years of age * history of coronary artery disease * history of peripheral artery disease * atrial fibrillation * heart failure * active immunosuppressive use * active infection * history of active malignancy * history of cerebrovascular event (ischemic/hemorrhagic) * Raynaud's phenomenon * renal transplant patients

Design outcomes

Primary

MeasureTime frameDescription
Correlation of serum sVE cadherin level and other measurementsApproximately 122 days were sufficient for patient recruitment for the study. After patient recruitment was completed, we followed the patients for approximately 844 days, monitoring their survival/death status.To investigate the relationship between sVE cadherin levels and ultrasonographic carotid intima-media thickness (CIMT), flow-mediated dilation(FMD), nailfold capillaroscopy(NC) test results measured in patients.
Distribution of sVE cadherin levels in the patient groupApproximately 122 days were sufficient for patient recruitment for the study. After patient recruitment was completed, we followed the patients for approximately 844 days, monitoring their survival/death status.sVE cadherin levels

Secondary

MeasureTime frameDescription
All-cause mortalityAfter patient recruitment was completed, we followed the patients for approximately 844 days, monitoring their survival/death status.Evaluation of those who died and those who survived after approximately over 2 years.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORAlper Alp, Assoc Prof,MD

Muğla Sıtkı Koçman University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026