Empagliflozin in Heart Failure Dialysis Patients

NCT ID: NCT05967156

Last Updated: 2025-06-06

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

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-06-01

Study Completion Date

2025-06-03

Brief Summary

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Empagliflozin is not still approved for glomerular filtration rate \< 20 cc/min/1.73m2. Considering the cardiac and renal benefits of this drug, the evaluation of the safety and efficacy of Empagliflozin for heart failure dialysis patients seems to be mandatory.

Detailed Description

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Heart failure dialysis patients with residual renal function will be followed up on Empagliflozin based on echocardiographic parameters, pro-brain natriuretic peptide levels, diuresis volume, and serum acidity.

Conditions

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Heart Failure Hemodialysis

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Empagliflozin

Heart failure dialysis patients will be treated with Empagliflozin

Group Type EXPERIMENTAL

Empagliflozin10Mg Tab

Intervention Type DRUG

10 mg daily

Interventions

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Empagliflozin10Mg Tab

10 mg daily

Intervention Type DRUG

Other Intervention Names

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Abide

Eligibility Criteria

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Inclusion Criteria

* Heart failure on dialysis with residual renal function

Exclusion Criteria

* Dialysis patients with no residual urine
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shahid Beheshti University of Medical Sciences

OTHER

Sponsor Role lead

Responsible Party

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nooshin dalili

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Dalili

Role: PRINCIPAL_INVESTIGATOR

SMBU

Locations

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Nooshin Dalili

Tehran, , Iran

Site Status

Countries

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Iran

Other Identifiers

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SBMU--

Identifier Type: -

Identifier Source: org_study_id

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