Efficacy of Intralesional Sodium Thiosulfate Versus Intralesional Saline for Dystrophic and Idiopathic Calcinosis Cutis

Calcinosis Cutis Clinical Trial

Official 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

Status Terminated

Clinical Trial Summary

The purpose of our research is to compare the effectiveness of 125mg/50ml sodium thiosulfate (STS) solution to normal saline (0.9% sodium chloride) when injected intralesionally for the treatment of calcinosis cutis. Our specific aim is to assess the response of dystrophic and idiopathic calcinosis cutis to the injections of sodium thiosulfate in our patients.

Clinical Trial Description

Our specific aim is to assess the response of dystrophic and idiopathic calcinosis cutis to the injections of sodium thiosulfate in our patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03639779
Study type	Interventional
Source	University of Central Florida
Contact
Status	Terminated
Phase	Phase 4
Start date	November 2, 2018
Completion date	December 31, 2019

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See also
Status	Clinical Trial	Phase
Withdrawn	`NCT01918904` - A Pilot Study to Evaluate Topical Sodium Thiosulfate Therapy for Calcinosis Cutis	Phase 2
Not yet recruiting	`NCT05870852` - Effectiveness of ESWT and PNF in Scleroderma With Calcinosis	N/A
Not yet recruiting	`NCT03972566` - Localized Effects of PBM and Exogenous NO on CREST Patients Calcinosis Cutis & Raynaud Phenomenon