PyroCal-greffe: Determinants of Vascular Calcification in Chronic Renal Failure : Impact of Pyrophosphate Levels After Renal Transplantation

Sponsor
Centre Hospitalier Universitaire de Nice (Other)
Overall Status
Unknown status
CT.gov ID
NCT03462238
Collaborator
(none)
60
1
2
10.1
6

Study Details

Study Description

Brief Summary

Arterial calcifications (AC) are constant lesions in patients with Chronic Kidney Diseases (CKD). Renal transplantation would reduce their progression compared to dialysis. AC pathophysiology is a complex and finely regulated process that involves many local and systemic factors, both pro- and anti-calcification. The progression of the CKD is accompanied by an increase in phosphate levels as the renal excretion capacity of inorganic phosphates (Pi) decreases while their digestive absorption remains unchanged. Hyperphosphatremia is a well-identified calcifying factor contributing to ACs in the CKD. On the other hand, pyrophosphate (PPi) is an anti-calcifying factor from the hydrolysis of extracellular ATP by ectonucleotidases. While there are many factors that may contribute to a protective effect against AC progression of renal transplantation, no study has been yet analysed the role of PPi. Plasma concentration of PPi is decreased in dialysis patients compared to non-kidney failure patients.

The main objective of this monocentric, prospective and interventional pilot study will be to compare the progression of CA and [PPi]pl between a group of renal transplant patients over the past 24 months and a group of dialysis patients over the same period of time. The secondary objectives will be to compare the progression of ACs and the ratio[PPi]pl/[Pi]pl between transplanted and dialysis patients. Transplanted patients will be included within 24 (±3) months of transplant. Dialysis patients will be included at 24 (±3) months of the CT scan performed during the pre-transplant check-up. At inclusion, all patients will benefit from a CT scan without injection and a plasma dose of PPi, Pi and other factors involved in controlling calcification.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Blood collection for Ppi assay
  • Radiation: CT Scan
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Determinants of Vascular Calcification in Chronic Renal Failure : Impact of Pyrophosphate Levels After Renal Transplantation
Anticipated Study Start Date :
Apr 1, 2018
Anticipated Primary Completion Date :
Feb 1, 2019
Anticipated Study Completion Date :
Feb 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Other: Kidney transplant patients

Group of renal transplant patients for 24 months

Procedure: Blood collection for Ppi assay
A 4.5 ml blood sample will be taken with a citrate vacuum tube.

Radiation: CT Scan
A scanner will be performed

Other: Dialysis patients

Group of dialysis patients for 24 months

Procedure: Blood collection for Ppi assay
A 4.5 ml blood sample will be taken with a citrate vacuum tube.

Radiation: CT Scan
A scanner will be performed

Outcome Measures

Primary Outcome Measures

  1. Concentration of plasma PPi [at patient inclusion]

  2. Calcification score [at patient inclusion]

    The calcification score is based on a computed tomography (CT) scan.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Kidney transplant patients for 24 (±3) months or dialysis patients who have performed pre-transplant CT for 24 (±3) months

  • Major Patients

  • Informed patients who have signed informed consent

  • Patients of both sexes

  • Patients affiliated to the social security system

Exclusion Criteria:
  • Pregnancy in progress (checked by a previous ßHCG pregnancy test)

  • Patients whose clinical condition would not allow inclusion in the study.

  • Patients not affiliated with social security

  • Patients not consenting or unable to understand the protocol and its development

  • Progressive cancer pathology

  • Patients under guardianship, under curatorship, protected by law

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hôpital Pasteur - Unité d'Exploration Fonctionelle Vasculaire Nice France 06001

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nice

Investigators

  • Principal Investigator: Georges LEFTHERIOTIS, PU-PH, Centre Hospitalier Universitaire de Nice

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nice
ClinicalTrials.gov Identifier:
NCT03462238
Other Study ID Numbers:
  • 17-AOI-02
First Posted:
Mar 12, 2018
Last Update Posted:
Mar 12, 2018
Last Verified:
Mar 1, 2018
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 12, 2018