Cairo University
Cairo, Egypt
Location status: Recruiting
NCT Number: NCT07076615
This randomized controlled trial evaluates the efficacy and tolerability of early initiation of dapagliflozin in adult patients hospitalized with acute heart failure (AHF). The study aims to assess the effect of dapagliflozin on pulmonary congestion as measured by lung ultrasound (LUS), length of hospital stay, and cardiac and renal biomarkers. A total of 100 patients will be randomized into two groups: one receiving dapagliflozin plus diuretics and the other receiving diuretics alone. Key outcomes include the reduction of extravascular lung water (assessed by B-lines in LUS), improved diuretic response, changes in NT-proBNP, sST2, CA-125, and NGAL levels, and incidence of acute kidney injury. The study will be conducted at the Cardiology and ICU departments at Kasr Al Ainy Hospital, Cairo University
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 4
Cairo, Egypt
Location status: Recruiting
Acute Heart Failure (AHF) is a life-threatening syndrome and a leading cause of hospitalization worldwide. Effective decongestion during AHF episodes is essential for improving patient outcomes and reducing hospital readmissions. Sodium-glucose co-transporter 2 (SGLT2) inhibitors, particularly dapagliflozin, have shown significant promise in improving cardiovascular outcomes in chronic heart failure; however, their role during acute episodes remains under active investigation.
This prospective, randomized controlled trial aims to assess the efficacy and safety of early dapagliflozin initiation in hospitalized adult patients with AHF, irrespective of diabetes status. A total of 100 patients admitted to the Cardiology and Intensive Care Departments of Kasr Al Ainy Hospital, Cairo University, will be enrolled and randomized (1:1) to either standard diuretic therapy alone or dapagliflozin (10 mg once daily) plus diuretics.
The study's primary endpoint is the degree of pulmonary congestion, evaluated through lung ultrasound (LUS) using an 8-zone scanning protocol and quantification of B-lines. Secondary outcomes include hospital length of stay, diuretic response, changes in cardiac biomarkers (NT-proBNP, sST2, and CA-125), renal biomarker NGAL, and incidence of acute kidney injury.
LUS and echocardiography will be performed by certified intensivists using standardized protocols. Biomarkers will be measured via ELISA kits at three time points: within 24 hours of admission, and at discharge.
The hypothesis is that early use of dapagliflozin in AHF enhances decongestion, improves natriuretic response, and enables earlier hospital discharge without increasing adverse renal or metabolic events.
The results of this study will provide valuable insights into the use of SGLT2 inhibitors during the acute phase of heart failure and may inform future clinical practice guidelines.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Receives dapagliflozin 10 mg once daily + standard intravenous diuretic therapy
Arm B (Control Group): Receives standard intravenous diuretic therapy alone
Time frame: Day 1 (Baseline) Day 3 within 24 hours prior to hospital discharge (mean 7 days post-admission)
To evaluate the effect of dapagliflozin on pulmonary congestion in patients hospitalized with acute heart failure, using lung ultrasound to measure the number of B-lines at defined intervals during hospitalization.
Time frame: From hospital admission to hospital discharge (an average of 7 days)
To assess the effect of dapagliflozin on the duration of hospitalization, measured in total days from admission to discharge.
Time frame: Baseline (within 24 hours of admission), and within 24 hours prior to hospital discharge (mean 7 days)
To assess the effect of dapagliflozin on renal injury using the neutrophil gelatinase-associated lipocalin (NGAL) level in ng/mL as a renal biomarker.
Time frame: Baseline (within 24 hours of admission), and within 24 hours prior to hospital discharge (mean 7 days)
To assess the change in NT-proBNP levels (pg/mL) in patients receiving dapagliflozin during hospitalization for acute heart failure.
Time frame: Day 1, Day 2, and Day 3 of hospitalization
To determine the net fluid balance (fluid input minus output) (mL per 24 hours) to evaluate diuretic efficiency in patients receiving dapagliflozin.
Time frame: From admission (Day 1) through hospital discharge (up to 14 days)
To determine the incidence of acute kidney injury (AKI) according to KDIGO guidelines in patients receiving dapagliflozin during hospitalization.
Time frame: Baseline (within 24 hours of admission), and within 24 hours prior to hospital discharge (mean 7 days)
To evaluate the effect of dapagliflozin on soluble ST2 (sST2) (ng/mL) concentrations in patients with acute heart failure.
Time frame: Baseline (within 24 hours of admission), and within 24 hours prior to hospital discharge (mean 7 days)
To measure the change in CA-125 (Cancer Antigen 125) levels (U/mL) in patients treated with dapagliflozin during hospitalization for acute heart failure.
Contact information is provided by the study sponsor or research team.
Ahmed M Kamal, Lecturer of Cardiovascular
CONTACT
May M Abdalla, Senior teaching assistant
CONTACT
May Mohamed Abdalla
Other
Acronym: Dapagliflozin
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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