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Clinical trial

A Comparative Study of the Efficacy of Intralesional Sodium Thiosulfate Versus Intralesional Normal Saline for the Treatment of Dystrophic and Idiopathic Calcinosis Cutis, A Double-Blind Randomized Placebo-Controlled Trial

NCT03639779 is registered in ClinicalTrials.gov with University of Central Florida as lead sponsor.

NCT NCT03639779
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Registry record

As filed in ClinicalTrials.gov.

Title
A Comparative Study of the Efficacy of Intralesional Sodium Thiosulfate Versus Intralesional Normal Saline for the Treatment of Dystrophic and Idiopathic Calcinosis Cutis, A Double-Blind Randomized Placebo-Controlled Trial
Lead sponsor
University of Central Florida
Phase
Phase 4
Overall status
Terminated
Start date
November 2, 2018
Completion date
December 31, 2019
Enrollment
5 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

calcinosis cutis