EMPAgliflozin in Heart Failure With PReserved Ejection Fraction and End Stage Renal Disease

NCT ID: NCT06249945

Last Updated: 2024-12-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE4

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-03-05

Study Completion Date

2030-12-31

Brief Summary

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The presence of CKD has been linked to the development of HFpEF. Currently, the treatment for HFpEF is limited. SGLT2i are one of the few drug classes that have proven efficacy in HFpEF in randomized controlled trials. The results of mechanistic studies suggest that the benefits of SGLT2i on diastolic heart failure are independent of their glycosuric actions and may still be present in anuric subjects. Despite the significance of HFpEF in patients with CKD, patients with advanced kidney disease have been excluded from studies investigating anti-heart failure drugs. The effects of SGLT2i in patients under maintenance dialysis are largely unknown. Past pharmacokinetics and pharmacodynamics studies on empagliflozin in patients with end-stage renal disease (ESRD) demonstrated that the use of empagliflozin in patients with ESRD seemed safe, yet its efficacy remains to be explored.

Detailed Description

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Conditions

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Heart Failure With Preserved Ejection Fraction End Stage Renal Disease on Dialysis

Keywords

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end-stage renal disease sodium-glucose co-transporter 2 inhibitors heart failure diastolic function empagliflozin

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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empagliflozin

Jardiance, 25 mg, QD, for 6 months

Group Type EXPERIMENTAL

Empagliflozin 25 MG

Intervention Type DRUG

The medication will be packed in a customized sealed jar and labeled on the exterior of the jar.

Placebo

QD, for 6 months

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

The placebo tablet is manufactured by Prince Pharmaceutical Co., Ltd, a leading manufacturer of nutritional supplements with certifications including cGMP, GMP, ISO, and HACCP. The Prince Pharmaceutical also provides Original Equipment Manufacturing (OEM)/Original Design Manufacturing (ODM) services for a wide array of tablet shapes, and post-processing techniques such as film coating and sugar coating.

Interventions

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Empagliflozin 25 MG

The medication will be packed in a customized sealed jar and labeled on the exterior of the jar.

Intervention Type DRUG

Placebo

The placebo tablet is manufactured by Prince Pharmaceutical Co., Ltd, a leading manufacturer of nutritional supplements with certifications including cGMP, GMP, ISO, and HACCP. The Prince Pharmaceutical also provides Original Equipment Manufacturing (OEM)/Original Design Manufacturing (ODM) services for a wide array of tablet shapes, and post-processing techniques such as film coating and sugar coating.

Intervention Type DRUG

Other Intervention Names

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Jardiance 25 MG

Eligibility Criteria

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Inclusion Criteria

* Age ≥20 years old
* ESRD under chronic, maintenance dialysis with stable dry weight for the past 6 months
* Prior diagnosis of HFpEF, as defined by a score of ≥5 on the HFA-PEFF diagnostic algorithm.

Exclusion Criteria

* Age \<20 years old
* Ongoing pregnancy
* NYHA class IV heart failure
* Any hospitalization for heart failure within the past month Ongoing acute urinary tract infection at the time of screening
* Known acute genital infection
* Severe peripheral artery disease (Rutherford category 4-6)
* Acute coronary syndrome, stroke or transient ischemic attack within the past month
* Recent initiation of chronic maintenance hemodialysis within 6 months
* Adjustment of dry weight with changes greater than 5% of body weight within the past month
* Documented left ventricular ejection fraction =\<40% by any imaging modality within 1 month of screening
* Refused informed consent
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shin Kong Wu Ho-Su Memorial Hospital

OTHER

Sponsor Role collaborator

National Taiwan University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Donna SH Lin, MD

Role: PRINCIPAL_INVESTIGATOR

Shin Kong Wu Ho-Su Memorial Hospital

Chih-Cheng Wu, MD. PhD

Role: PRINCIPAL_INVESTIGATOR

National Taiwan University Hsin-Chu Hospital

Locations

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National Taiwan University Hospital Hsinchu Branch

Hsinchu, , Taiwan

Site Status RECRUITING

Shin Kong Wu Ho-Su Memorial Hospital

Taipei, , Taiwan

Site Status RECRUITING

Countries

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Taiwan

Central Contacts

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Donna SH Lin, MD

Role: CONTACT

Phone: +886912902379

Email: [email protected]

Hao-Yun Lo, MD

Role: CONTACT

Phone: +886972234640

Email: [email protected]

Facility Contacts

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Chih-Cheng Wu, PhD

Role: primary

Donna SH Lin, MD

Role: primary

References

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Other Identifiers

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202301126MINC

Identifier Type: -

Identifier Source: org_study_id