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The Effect of dapagliflozin on hemodynamics in patients with acute heart failure complicated with type 2 diabetes

The Effect of dapagliflozin on hemodynamics in patients with acute heart failure complicated with type 2 diabetes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017353
Enrollment
Unknown
Registered
2018-07-25
Start date
2018-08-01
Completion date
Unknown
Last updated
2018-07-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hearrt Failure

Interventions

Group 1:dapagliflozin 10 mg + insulin

Sponsors

Shanghai Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Provide a signed and dated informed consent form; (2) Male or female, age = 18 years old; (3) Acute decompensation or acute new heart failure in chronic heart failure; (4) BNP or NT-pro BNP values are elevated; (5) Previously diagnosed as type 2 diabetes; (6) eGFR = 30mL / min / 1.73m3 at the time of registration; (7) Patients should receive standard background care for acute heart failure and follow local approved guidelines; (8) Subjects indicated willingness and completion of all steps and study intervention cycles in the study.

Exclusion criteria

Exclusion criteria: (1) receiving SGLT2 inhibitor treatment or previous intolerance to SGLT2 inhibitor within 8 weeks prior to enrollment; (2) implanting CRT 3 months ago or planning to implant CRT in the near future; (3) severe valvular disease; (4) Perform an orthotopic heart transplant or install a ventricular assist device within 12 months; (5) complex congenital heart disease; (6) Symptomatic bradycardia or second or third degree heart block without a pacemaker; (7) End-stage renal disease requiring replacement therapy; (8) Non-cardiogenic end-stage diseases with a predicted survival period of no more than 12 months; (9) pregnancy or planned pregnancy; (10) Failure to follow the research plan; (11) Other research projects that have been enrolled or planned to be enrolled; (12) Disagree to participate in the study.

Design outcomes

Primary

MeasureTime frame
Cardiac index;Intrathoracic blood volume;Extravascular lung water;

Secondary

MeasureTime frame
Changes of other hemodynamic parameters;Fasting plasma glucose;BNP/NT-pro BNP;LVEF;

Countries

China

Contacts

Public ContactMin Zhang

Shanghai Chest Hospital

zhangminxk@126.com+86 18017320207

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026