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Sodium-glucose Cotransporter Type 2 Inhibitors for Acute Cardiorenal Syndrome Prevention - Trial NCT04778787

Access comprehensive clinical trial information for NCT04778787 through Pure Global AI's free database. This Phase 4 trial is sponsored by I.M. Sechenov First Moscow State Medical University and is currently Recruiting. The study focuses on Congestive Heart Failure. Target enrollment is 100 participants.

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NCT04778787
Phase 4
Recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT04778787
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Sodium-glucose Cotransporter Type 2 Inhibitors for Acute Cardiorenal Syndrome Prevention
Impact of Sodium-glucose Cotransporter Type 2 Inhibitors on the Course of Cardiorenal Syndrome in Acute Decompensation of Chronic Heart Failure

Study Focus

Congestive Heart Failure

Standard list of drugs used for acute decompensation of CHF (loop diuretics, vasodilators, digoxin, inotropic agents, vasopressors), plus dapagliflozin (Forxiga; MP-002596)

Interventional

drug

Sponsor & Location

I.M. Sechenov First Moscow State Medical University

Moscow,Moscow, Russian Federation

Timeline & Enrollment

Phase 4

Jan 01, 2021

Jan 01, 2022

100 participants

Primary Outcome

admission to the intensive care unit due to worsening heart failure during the current hospitalization,death due to heart failure

Summary

The effect of sodium-glucose cotransporter type 2 inhibitors (SGLT2i) on the parameters of
 renal function in acute decompensation of chronic heart failure (CHF) compared to standard
 therapy will be analyzed. Based on the dynamics of the clinical condition, the duration of
 hospitalization, and blood biochemical parameters (creatinine, urea, uric acid, potassium,
 sodium, N-terminal pro-brain natriuretic peptide NT-proBNP) conclusions will be drawn about
 the possibility of using SGLT2i in this group of patients.

ICD-10 Classifications

Congestive heart failure
Heart failure
Hypertensive heart disease with (congestive) heart failure
Hypertensive heart and renal disease with (congestive) heart failure
Heart failure, unspecified

Data Source

ClinicalTrials.gov

NCT04778787

Non-Device Trial