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Clinical Trials in the EU / 2026-525680-41-00
Authorised Phase II

Attenuating Calciprotein particles Transformation and Inhibiting Vascular calcification Evolution by Sodium ThioSulphate trial

2026-525680-41-00 · tracked via the Priya Life Science EU tracker
Sponsor
Radboud universitair medisch centrum Stichting
Sponsor type
Hospital/Clinic/Other health care facility
Therapeutic area
Therapeutics
Decision date
11/09/2026
Enrollment target
40
Sites
Netherlands

Condition studied

Vascular Calcification

Investigational medicinal product(s)

Natriumthiosulfat 25%

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Difference in pre to post-dialysis change in T₅₀ between the non-dosed session and the STS-dosed session in the same participant., Change in pre-dialysis T₅₀ from the non-dosed control session to each of the three STS-dosed sessions

Endpoint detail

Within subject differences in CPP amounts between non-dosed and STS-dosed sessions and the STS-dosed sessions, and in pre- to post-dialysis changes within each session., Correlations between changes in T₅₀ and CPP measures across session and timepoints., Within-subject changes in CRP, IL-6, TNF-α and NO/ROS related markers between sessions., Changes in P1NP, CTX, osteocalcin, ALP, bone-specific ALP, phosphate, calcium, PTH, and FGF23 between sessions and timepoints.

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2026-525680-41-00 on CTIS ↗ ← All trials in the EU