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DApagliflozin Cardiovascular Effects on Patients at End-stage REnal Disease (Dare-Esrd)

Primary Purpose

End-stage Kidney Disease

Status
Recruiting
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Dapagliflozin
Sponsored by
University of Campinas, Brazil
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End-stage Kidney Disease

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 18 years or older On regular dialysis regimen for at least 3 months Exclusion Criteria: Known allergy to any of the investigational drug components Current use of sodium-glucose co-transporter 2 inhibitors Pregnant woman Myocardial infarction or myocardial revascularization in the past 3 months

Sites / Locations

  • Centro de Pesquisas ClínicasRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Dapagliflozin

Control

Arm Description

Dapagliflozin 10mg P.O. daily for 6 months add-on to standard treatment

No intervention. Patients will be followed for 6 months on their standard treatment.

Outcomes

Primary Outcome Measures

NT-proBNP
Difference between groups in NT-proBNP change from baseline

Secondary Outcome Measures

Echocardiography
Difference between groups from baseline of the following: ejection fraction, e/e' ratio, global longitudinal and radial strain and indexed left ventricle mass

Full Information

First Posted
January 5, 2023
Last Updated
October 20, 2023
Sponsor
University of Campinas, Brazil
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1. Study Identification

Unique Protocol Identification Number
NCT05685394
Brief Title
DApagliflozin Cardiovascular Effects on Patients at End-stage REnal Disease
Acronym
Dare-Esrd
Official Title
Dapagliflozin Cardiovascular Effects on Patients at End-stage Renal Disease
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 24, 2023 (Actual)
Primary Completion Date
November 1, 2023 (Anticipated)
Study Completion Date
February 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Campinas, Brazil

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Treatment with sodium glucose co-transporter type 2 inhibitors (Sglt2i) reduced the incidence of cardiovascular death and hospitalization for heart failure by 29% in individuals with moderate chronic kidney disease. Recent observations found that beyond its effect on natriuresis, Sglt2i directly interacts with cardiomyocytes inducing improvement of myocardial function. This effect is not mitigated as glomerular filtration rate declines. Therefore, plausibly treatment with Sglt2i may attenuate heart failure in individuals end-stage kidney disease (ESKD) requiring dialysis, in whom cardiovascular disease remains the leading cause of death. In this context, this project was designed to estimate the effect of dapagliflozin on myocardial function of dialysis subjects. Individuals with diagnosed ESKD on dialysis for at least 3 months, from both sexes, aged more than 18 years of age are eligible. Exclusion criteria are pregnant woman, hepatic failure, and known allergy to study medications. Eligible patients will be recruited from the Nephrology Division of the Clinics Hospital of the University of Campinas (Unicamp). The study was designed as a prospective, randomized, open-label, phase 4 clinical trial. Patients will be randomized, 1:1, for a 6-months treatment with either dapagliflozin 10mg/day (n=40) add to standard treatment or standard treatment alone (n=40). At the randomization visit, all patients will undergo a detailed interview and medical examination by the physician-researcher, echocardiogram and blood samples will be collected for further biochemical analysis and follow up visits will be scheduled every month for endpoints disclosure and medications dispensation until the end of study participation at the 6th month visit when echocardiogram and blood sample collection will be repeated. Primary goal will be the difference between groups in mean change of NTproBNP levels during treatment. Secondary endpoints encompass the mean change in ejection fraction, e/e' ratio, global longitudinal and radial strain and indexed left ventricle mass. Changes in bone metabolsm and structure, assessed by serum levels of FGF-23 and α-Klotho, and changes in bone mineral density will be compared between groups as an exploratory analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-stage Kidney Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Prospective, randomized, open-label, controlled trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Dapagliflozin
Arm Type
Experimental
Arm Description
Dapagliflozin 10mg P.O. daily for 6 months add-on to standard treatment
Arm Title
Control
Arm Type
No Intervention
Arm Description
No intervention. Patients will be followed for 6 months on their standard treatment.
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin
Intervention Description
Dapagliflozin 10mg P.O. daily
Primary Outcome Measure Information:
Title
NT-proBNP
Description
Difference between groups in NT-proBNP change from baseline
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Echocardiography
Description
Difference between groups from baseline of the following: ejection fraction, e/e' ratio, global longitudinal and radial strain and indexed left ventricle mass
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years or older On regular dialysis regimen for at least 3 months Exclusion Criteria: Known allergy to any of the investigational drug components Current use of sodium-glucose co-transporter 2 inhibitors Pregnant woman Myocardial infarction or myocardial revascularization in the past 3 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joaquim Barreto, MD
Phone
+55 19 3521 7959
Email
joaquimbarretoantunes@gmail.com
Facility Information:
Facility Name
Centro de Pesquisas Clínicas
City
Campinas
State/Province
SP
ZIP/Postal Code
13083610
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
joaquim b oliveira, md
Phone
+55 19 35217959

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Unidentified data may be shared on reasonable request.

Learn more about this trial

DApagliflozin Cardiovascular Effects on Patients at End-stage REnal Disease

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