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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04950439
Other study ID # 19-API-02
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 14, 2022
Est. completion date March 14, 2028

Study information

Verified date September 2023
Source Centre Hospitalier Universitaire de Nice
Contact Favre Guillaume, PhD
Phone 0492038428
Email favre.g@chu-nice.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Arterial calcifications start at early stages of chronic kidney disease (CKD) and are associated to cardiovascular mortality. Pyrophosphate (PPi) is an endogenous compound, which stops the mineralization process in bones and is expected to act at ectopic sites. In uremic rats, low PPi plasma levels are associated with high calcium content in the aorta and peritoneal administration of PPi blocks this process. People on maintenance dialysis or kidney transplant recipients have low plasma levels of PPi and show high scores of arterial calcification. The purpose is to determine the role of low PPi in the development of arterial calcifications in patients with CKD stage 3 or 4. To that aim, 252 patients with eGFR between 59 et 20 ml/min/1,73 m2 will be recruited and will be examined at baseline and three years later.


Recruitment information / eligibility

Status Recruiting
Enrollment 242
Est. completion date March 14, 2028
Est. primary completion date March 14, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - eGFR between 59 et 20 ml/min/1,73 m2 twice at three month interval Exclusion Criteria: 1. kidney transplantation 2. acute inflammatory disease or active cancer

Study Design


Intervention

Other:
Collect blood sample
A blood sample dedicated to the study and necessary for routine care is taken. The pulse wave velocity and systolic pressure index are measured. A myocardial CT scan coupled with a computed tomography is performed. The patient collects stools at his home, simply conditions them and sends them by mail to the centre, which stores them.

Locations

Country Name City State
France CHU de Nice Nice Alpes Maritimes

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Plasma levels of PPI To show that low plasma levels of PPi at baseline is associated with a high progression of arterial calcification at three years after adjustment for confounding variables 3 years
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