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Clinical Trial Summary

Observational cohort randomized controlled study to study the influence of correction of ID by intravenous injection of ferric carboxymaltose (Ferinject®) on quality of life indicators, functional status in a cohort of patients with HFpEF.


Clinical Trial Description

The prevalence of HFpEF among patients admitted to cardiology hospitals will be studied. The study will include patients with NYHA II-III who have signed an informed consent that meets the inclusion/exclusion criteria. The effectiveness of intravenous administration of iron carboxymaltose (Ferinject ® ) to correct iron deficiency and improve the clinical course of HFpEF will be evaluated. A group without iron deficiency will be recruited as a control group (n=30). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05793996
Study type Interventional
Source Tomsk National Research Medical Center of the Russian Academy of Sciences
Contact Olga V. Tukish, Ph.D.
Phone +79069476343
Email olgatukish@yandex.ru
Status Recruiting
Phase Phase 4
Start date April 28, 2023
Completion date December 2026

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