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NCT05262764Completed

Post Marketing Surveillance (PMS) of JARDIANCE in Chronic Heart Failure (CHF)

Post Marketing Surveillance on Long Term Drug Use of JARDIANCE® Tablets in Patients With Chronic Heart Failure in Japan

Source: ClinicalTrials.gov · Last updated 24 Mar 2026

Brief summary (registry, in English)

Study objective is to investigate the safety and effectiveness of long-term daily use of JARDIANCE® Tablets in patients with chronic heart failure (CHF) under real-world use.

Status (registry)
Completed
Study type
Observational
Enrollment
1200 (actual)
First submitted
1 Mar 2022
Start date
15 Apr 2022
Primary completion date
21 Jun 2024
Lead sponsor
Boehringer Ingelheim
NCT number
NCT05262764

What you commit to

  • Study type: Observational
  • Participants enrolled: 1200
  • From 15 Apr 2022 to the primary completion date, 21 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • None

Who the study is looking for

  • Patients with chronic heart failure (CHF) failure who are prescribed with JARDIANCE® Tablets in Japan
  • Patients who have never been treated with Empagliflozin (including treatment for type 2 diabetes mellitus (T2DM)) before enrolment

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Nippon Boehringer Ingelheim Co., Ltd.
Coordinator of this site? Confirm its status
TokyoJapanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.