Extracellular Vesicles as Biomarkers for Chronic Renal Failure (VE-IRC)
Primary Purpose
Chronic Renal Failure, Urinary Extracellular Vesicle
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
urinary extracellular vesicle concentration
blood sample
Sponsored by
About this trial
This is an interventional basic science trial for Chronic Renal Failure focused on measuring urinary extracellular vesicle, Chronic Renal Failure
Eligibility Criteria
Inclusion Criteria:
- subject > 18 years old
- healthy subjects : no medical history, in particular cardiovascular, without drug treatment, without proteinuria, normal BMI
- CRF patients : eGFR estimated according to the MRDR formula less than 89 mL/min/1,73m²
Exclusion Criteria:
- patients under dialysis protocols
- renal transplant patients
Sites / Locations
- CHU Amiens
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
healthy subject
CRF patients
Arm Description
healthy subjects : no medical history, in particular cardiovascular, without drug treatment, without proteinuria, normal BMI
CRF patients : eGFR estimated according to the MRDR formula less than 89 mL/min/1,73m²
Outcomes
Primary Outcome Measures
variation of urinary extracellular vesicle concentration between both groups
variation of urinary extracellular vesicle concentration between both groups : healthy and CRF patients Urinary extracellular vesicle concentrations will be measured as number of extracellular vesicles per mL of urine
Secondary Outcome Measures
Full Information
NCT ID
NCT04700631
First Posted
January 6, 2021
Last Updated
July 18, 2023
Sponsor
Centre Hospitalier Universitaire, Amiens
1. Study Identification
Unique Protocol Identification Number
NCT04700631
Brief Title
Extracellular Vesicles as Biomarkers for Chronic Renal Failure
Acronym
VE-IRC
Official Title
Extracellular Vesicles as Biomarkers for Chronic Renal Failure
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
July 1, 2023 (Actual)
Study Completion Date
July 1, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire, Amiens
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The recent discovery of extracellular vesicles (EV) as a mechanism of intercellular communication has made it possible to develop a new field of health research and could bring new information on the pathological mechanisms of renal diseases. Definition of physiologic and pathologic values of urinary extracellular vesicles (EVu) between healthy subjects and chronic kidney diseases (CKD) patients could be a new tool for follow up of renal diseases. EV are found in all biological fluids including urine, that's why they are increasingly analyzed in renal pathologies. The main objective of this study is to determine the physiological values and the pathological thresholds of EVu.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Renal Failure, Urinary Extracellular Vesicle
Keywords
urinary extracellular vesicle, Chronic Renal Failure
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
143 (Actual)
8. Arms, Groups, and Interventions
Arm Title
healthy subject
Arm Type
Active Comparator
Arm Description
healthy subjects : no medical history, in particular cardiovascular, without drug treatment, without proteinuria, normal BMI
Arm Title
CRF patients
Arm Type
Experimental
Arm Description
CRF patients : eGFR estimated according to the MRDR formula less than 89 mL/min/1,73m²
Intervention Type
Diagnostic Test
Intervention Name(s)
urinary extracellular vesicle concentration
Intervention Description
urinary extracellular vesicle concentration will be determined in urine samples from CRF and healthy patients
Intervention Type
Diagnostic Test
Intervention Name(s)
blood sample
Intervention Description
blood sample in order to determine creatin level
Primary Outcome Measure Information:
Title
variation of urinary extracellular vesicle concentration between both groups
Description
variation of urinary extracellular vesicle concentration between both groups : healthy and CRF patients Urinary extracellular vesicle concentrations will be measured as number of extracellular vesicles per mL of urine
Time Frame
one day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
subject > 18 years old
healthy subjects : no medical history, in particular cardiovascular, without drug treatment, without proteinuria, normal BMI
CRF patients : eGFR estimated according to the MRDR formula less than 89 mL/min/1,73m²
Exclusion Criteria:
patients under dialysis protocols
renal transplant patients
Facility Information:
Facility Name
CHU Amiens
City
Amiens
ZIP/Postal Code
80480
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Extracellular Vesicles as Biomarkers for Chronic Renal Failure
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