Skip to main content
OpenTrials
Completed

NCT Number: NCT03464149

The Longitudinal PTH-Study

The main study aim is to quantify the agreement between the analytical results provided by two third generation and two second generation Parathyroid hormone (PTH) assays. The primary comparison will be performed between the second-generation PTH assay"Intact PTH assay" from Siemens Healthcare Diagnostics Inc. and the third-generation PTH assay "biointact (1-84)" from Roche Diagnostics in terms of a Bland-Altman analysis. Several studies have evaluated the correlation between various PTH assays at a single time-point, but no previous study has tested the hypothesis that longitudinal changes in PTH levels, which are important for making treatment decisions, can be monitored by several PTH assays alike. To this aim, the key secondary objective is to analyze the longitudinal variance in PTH over the course of 1 year, using each of two assays of the second and third generations, respectively. Other secondary objectives include determining changes in serum phosphate, serum calcium, fibroblast growth factor 23 (FGF23), with respect to treatment decisions. For clinical applicability of the results to be obtained here, an important goal of the present study will be not to influence treatment decisions, which will remain independent of the study investigators, at the full responsibility of the hemodialysis physicians.

At every quarterly blood draw over the course of one year, the investigators will freeze the serum from 100 patients, and at the end of 4 quarters the investigators will analyze PTH-levels using the following assays: Intact Parathyroid Hormone (Advia Centaur, Siemens Healthcare), PTH-Intact (Cobas, Roche), PTH (1-84) - The agreement between the PTH assays will be analyzed at baseline, as well as at the subsequent quarterly evaluation time-points by Bland-Altman analysis and complemented by Passing-Bablok regression. The longitudinal changes in PTH will be displayed graphically and analyzed by estimating the within-patient variance across time, the between patient variance at each time-point as well as effects on the mean log-PTH level due to course of disease and therapeutic interventions from a linear mixed model.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients who were undergoing uninterrupted hemodialysis or hemodiafiltration at the Chronic Hemodialysis Unit of the Division of Nephrology and Dialysis, Medical University of Vienna between November 1st, 2017 and December 31st, 2018.
  • Existence of residual blood samples from four successive quarterly routine controls
  • Age ≥ 18 years
  • The test result of the assay must not have any diagnostic value or therapeutic consequence for the patients included in this study.

Exclusion criteria

  • Death during the observational period (all patients must have lived through the 1-year period and must have all 4 quarterly blood draws performed on them).
  • Age <18 years

Treatment and study plan

One armed study, blood from each patient is analysed by four assays ( two 3rd generation and two 2nd generation assays)

Diagnostic Test

Intact PTH Assay (Siemens Healthcare Diagnostics Inc); LIAISON 1-84 PTH Assay (Diasorin); PTH (1-84), biointact (Roche Diagnostics); PTH, intact (Roche Diagnostics)

Primary outcomes

  1. Longitudinal change in PTH levels measured in [pg/ml]

    Time frame: Timepoints of four consecutive quarterly routine controls per patient (month 1; month 4 ; month 8, month 12)

    PTH levels as measured by the second and third generation assays

Secondary outcomes

  1. Longitudinal within-patient change of PTH levels in [pg/ml]

    Time frame: Timepoints of four consecutive quarterly routine controls per patient (month 1; month 4 ; month 8, month 12)

    Longitudinal within-patient variance of PTH over the course of 1 year, using each of two assays of the second and third generations, respectively.

  2. Serum Calcium levels

    Time frame: Timepoints of four consecutive quarterly routine controls per patient (month 1; month 4 ; month 8, month 12)

    Serum Calcium levels

  3. Serum Phosphate levels

    Time frame: Timepoints of four consecutive quarterly routine controls per patient (month 1; month 4 ; month 8, month 12)

    Serum Phosphate levels as measured by quarterly routine controls

  4. Fibroblast growth factor 23 (FGF23

    Time frame: Timepoints of four consecutive quarterly routine controls per patient (month 1; month 4 ; month 8, month 12)

    Fibroblast growth factor 23 (FGF23) as measured in quarterly routine controls

Sponsors and collaborators

Lead sponsor

Medical University of Vienna

Other

Registry information

Official study title

Intact Versus Biointact Assays for Longitudinal Assessment of Parathyroid Hormone - The Longitudinal PTH Study

Important dates

Study start
2018
Primary completion
2018
Study completion
2019
First posted
Mar 13, 2018
Registry last updated
Jun 25, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.