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Clinical Trial Summary

Patients after the Fontan operation at a single institution will be randomized to receive a standardized extract of Aesculus hippocastanum L. (horse chestnut) or placebo for 4 months in a crossover clinical trial. The primary outcome will be the mesenteric artery resistance measured by Dopple sonography.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04035317
Study type Interventional
Source Casa Espirita Terra de Ismael
Contact
Status Withdrawn
Phase Phase 2
Start date October 31, 2017
Completion date December 31, 2020

See also
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