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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01886950
Other study ID # s52091
Secondary ID
Status Recruiting
Phase N/A
First received June 12, 2013
Last updated October 24, 2017
Start date August 1, 2010
Est. completion date December 2018

Study information

Verified date October 2017
Source Universitaire Ziekenhuizen Leuven
Contact Pieter Evenepoel, MD, PhD
Phone 003216344591
Email pieter.evenepoel@uzleuven.be
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A study of the natural history of bone and mineral disease (BMD) in patients with end-stage renal disease before and after kidney transplantation


Description:

Disturbances of mineral and bone diseaeses are frequently observed in CKD patients. Renal osteodystrophy is the term to describe the bone abnormalities. Epidemiological data showed adynamic bone disease (ABD) is the most frequent bone disorder in CKD stage 5D diseases. Low PTH, diabetes mellitus, malnutrition, metabolic acidosis, hypogonadism and low 1,25(OH)2D vitamin D deficiency are known risk factors for ABD. Mounting experimental data point towards a role of protein-bound uremic retention molecules (p-cresyl sulfate and indoxyl sulfate) in the pathogenesis and progression of ABD. ABD is not only recognized as a risk factor for fractures but also for arterial calcification.

The aim of the present study is (1) to investigate the role of indoxyl sulfate and p-cresyl sulfate in the pathogenesis and progression of ABD and arterial calcification in CKD stage5 and (2) to investigate the influence of renal transplantation on bone and arterial metabolism.


Recruitment information / eligibility

Status Recruiting
Enrollment 250
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- eligible for renal transplantation and >18 years

Exclusion Criteria:

- use of biphosphonates within the 6 months before the study entry

Study Design


Locations

Country Name City State
Belgium UZ Leuven Gasthuisberg Leuven Vlaams-Brabant

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary bone turnover, as assessed by bone biopsy to investigate the role of indoxyl sulfate and p-cresyl sulfate in the pathogenesis and progression of ABD and arterial calcification in CKD stage5 at the start of the study
Primary Evolution of bone turnover, as assessed by bone biopsy to evoluation the evolution of bone turnover after succesfull renal transplantation after 1 year
Primary aortic calcification, as assessed by lumbar X-ray the assess the evolution of (the degree of) aortic calcification one year after succesfull renal transplantation 1 year
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