Real-world Study to Describe the Effectiveness and Safety Outcomes of Jardiance in Chinese Patients With Heart Failure and Preserved Ejection Fraction
Not yet recruiting
- Conditions
- Heart FailurePreserved Ejection Fraction
- Registration Number
- NCT07047508
- Lead Sponsor
- Boehringer Ingelheim
- Brief Summary
The main objective of the study is to describe the effectiveness and safety outcomes among Chinese hospitalized heart failure with preserved ejection fraction (HFpEF) patients initiating Jardiance® in the real-world setting.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 3000
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of the composite outcome of HHF (the first HHF after the index date) or CV death up to 2.5 years HHF=Hospitalization for Heart Failure CV=cardiovascular
- Secondary Outcome Measures
Name Time Method Incidence of CV death up to 2.5 years Occurrence of death from any cause up to 2.5 years Incidence of the HHF (the first HHF after the index date) up to 2.5 years
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie Jardiance's efficacy in Chinese HFpEF patients?
How does Jardiance compare to standard-of-care diuretics in managing HFpEF symptoms?
Which biomarkers are associated with improved outcomes in HFpEF patients treated with Jardiance?
What adverse events are commonly observed in HFpEF patients initiating Jardiance therapy?
Are there combination therapies involving Jardiance that enhance treatment outcomes for HFpEF?