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Investigate the differences between treating Chronic Kidney Disease - Mineral and Bone Disorder with an iron-containing phosphate binder or a calcium-containing phosphate binder in patients with Kidney Disease treated with dialysis .

Investigate the differences between treating Chronic Kidney Disease - Mineral and Bone Disorder with an iron-containing phosphate binder or a calcium-containing phosphate binder in dialysis patients. - MAVA

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2017-002096-26-DK
Enrollment
35
Registered
2017-06-22
Start date
2017-08-24
Completion date
Unknown
Last updated
2020-02-01

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

Conditions

Chronic Kidney Disease - Mineral and Bone Disorder (CKD-MBD), especially bone metabolism and blood vessel calcification MedDRA version: 20.0 Level: PT Classification code 10064848 Term: Chronic kidney disease System Organ Class: 10038359 - Renal and urinary disorders MedDRA version: 20.0 Level: HLT Classification code 10027425 Term: Metabolic bone dis

Interventions

Trade Name: Velphoro Product Name: Velphoro Pharmaceutical Form: Chewable tablet INN or Proposed INN: Velphoro CAS Number: 12134-57-5

Sponsors

Universitetsklinik for Nyresygdomme og Blodtryksforhøjelse, Regionshospitalet Holstebro; Hospitalsenheden Vest
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 35-65 years old hemodialysis patients Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 35 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Inability to give informed consent, pregnancy, lactation, not radically treated cancer, alcohol abuse or drug abuse. Within three months: fractures, AMI, TCI, kidney transplant or parathyroidectomy.

Design outcomes

Primary

MeasureTime frame
Main Objective: To investigate whether treatment with an iron- or calcium-containing phosphate binder can affect differently the results from 18F-NaF PET/CT, bALP, osteocalcin, FGF23 og OPG/RANKL ratio. Differences in the stiffness of blood vessel assessed with applanation tonometry. Finally, we investigate changes in calcium score (TBR) and iron status;Secondary Objective: "not applicable";Primary end point(s): SUVmax og Ki;Timepoint(s) of evaluation of this end point: At the end of the trail, when all subjects have completed and the blood samples and PET/CT- scans are analyzed

Secondary

MeasureTime frame
Secondary end point(s): Biomarkers: bALP, FGF23, osteocalcin and OPG/sRANKL ratio PET/CT: SUVmean, SUVpeak, SUVA50%, K1, K2, K3, K4 and calcium score (TBR). Iron parameters: p-iron, ferritin, transferrin. Applanation tonometry: Heart Rate Variability (HRV), aPWV og AIx/central blood pressure (PVA) ;Timepoint(s) of evaluation of this end point: At the end of the trail, when all subjects have completed and the blood samples and PET/CT- scans are analyzed

Countries

Denmark

Contacts

Public ContactMarie Houmaa Vrist

Universitetsklinik for Nyresygdomme og Blodtryksforhøjelse, Regionshospitalet Holstebro; Hospitalsenheden Vest

marvri@rm.dk004578436585

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026