Real-world Study to Describe the Effectiveness and Safety Outcomes of Jardiance in Chinese Patients With Heart Failure and Preserved Ejection Fraction

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBoehringer Ingelheim

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

At least 18 years of age

At least 6 months of data prior to the index date

Left ventricular ejection fraction (LVEF) > 40 %

N-terminal Pro-B-type natriuretic peptide (NT-proBNP) > 125 pg/mL or brain natriuretic peptide (BNP) ≥ 35 pg/mL

Disqualifiers

None

Trial population

Chines patients with a heart failure and preserved ejection fraction (HFpEF) diagnosis who initiate Jardiance® after 1st of March 2023

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

3,000 Participants
are grouped into 1 trial group
Group A: Heart failure and preserved ejection fraction patients

Trial outcomes

Primary outcomes

1

Incidence of the composite outcome of HHF (the first HHF after the index date) or CV death

HHF=Hospitalization for Heart Failure CV=cardiovascular

Time frame
up to 2.5 years

Secondary outcomes

1

Incidence of CV death

Time frame
up to 2.5 years
2

Incidence of the HHF (the first HHF after the index date)

Time frame
up to 2.5 years
3

Occurrence of death from any cause

Time frame
up to 2.5 years

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: