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Clinical Trial Summary

To evaluate the efficacy of Sodium Thiosulfate (STS) compared to placebo, in reducing analgesic requirement in subjects with calcific uremic arteriolopathy (CUA) during an initial 28-day treatment phase.


Clinical Trial Description

Efficacy of Sodium Thiosulfate (STS) compared to placebo, in reducing analgesic requirement in subjects with calcific uremic arteriolopathy (CUA) during an initial 28-day treatment phase. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02527213
Study type Interventional
Source Luitpold Pharmaceuticals
Contact
Status Terminated
Phase Phase 3
Start date January 30, 2015
Completion date August 29, 2016

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