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Clinical Trial Summary

60 patients admitted to this ICCU at the Sheba medical Center will be randomly divided in to 2 groups. one group will receive the conventional treatment while the second group will receive the conventional treatment plus oxytocin infusion for 48 hours. all participants will undergo echo and cMRI during hospitalization.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT03001635
Study type Interventional
Source Sheba Medical Center
Contact Anat Berkovitch, resident
Phone 972545746277
Email [email protected]
Status Not yet recruiting
Phase Phase 2/Phase 3
Start date January 2017

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