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Clinical Trial Summary

Hypothesis: Taurine, in combination with standard iron chelation therapy, is more effective than chelation therapy alone in reducing cardiac iron overload, oxidative stress and cardiac damage in β-Thalassemia. Protocol: Sixty subjects with transfusion dependent β-Thalassemia receiving deferasirox iron chelation therapy will be recruited and randomized in a 1:1 ratio to either (1) placebo and continuation of their iron chelation or (2) a combination of iron chelation plus taurine. Transfusion and safety visits will be scheduled monthly with clinical/biochemical assessment visits every three months. The efficacy of taurine combined with standard chelation therapy will be assessed at baseline and 12 months posttreatment by both cardiac T2*MRI, and cardiac function. The recruitment period is projected to be 12 months from initiation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04291352
Study type Interventional
Source University Health Network, Toronto
Contact Anneliesse Justiniano
Phone 416-340-4800
Email anneliesse.justiniano@uhn.ca
Status Recruiting
Phase N/A
Start date June 1, 2020
Completion date October 31, 2025

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