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The Effect of Addition of Metformin to SGLT2 In Diabetic Patients With Heart Failure With Preserved Ejection Fraction

Primary Purpose

Heart Failure With Preserved Ejection Fraction, Diabete Type 2

Status
Not yet recruiting
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Metformin
Sponsored by
October University for Modern Sciences and Arts
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure With Preserved Ejection Fraction focused on measuring metformin, SGLTi, HFpEF

Eligibility Criteria

40 Years - 74 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age of 40 years to 74 years. HFpEF (≥ 50%) Written informed consent of the subject to participate in the study. New York Heart Association functional class I-IV. Diabetic patients SGL-2 naive. Newly diagnosed heart failure of preserved ejection fraction Exclusion Criteria: Patients with heart failure with reduced ejection fraction (< 40%) Age less than 40 and more than 74 GFR < 30 mL/min A1c > 9 Known allergy to metformin End- stage liver disease Cancer Pregnancy or lactation

Sites / Locations

  • clinical research uint- El-sheikh zayed specialized hospital SMC- Egyptian Ministry of health

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

control(SGLT2i/ARBs/MRA/ +/- diuretics).

intervention

Arm Description

Lifestyle counseling plus standard evidence-based therapy for HFpEF (SGLT2i/ARBs/MRA/ +/- diuretics).

Lifestyle counseling plus standard evidence-based therapy for HFpEF (SGLT2i/ARBs/MRA/ +/- diuretics)+ metformin

Outcomes

Primary Outcome Measures

Hospitalization rate
Hospitalization rate
HRQOL using Minnesota Living with Heart Failure Questionnaire for quality-of-life evaluation (MLFHQ)
HRQOL using Minnesota Living with Heart Failure Questionnaire for quality-of-life evaluation (MLFHQ)

Secondary Outcome Measures

The change in the mean early diastolic mitral annular velocity (mean e'), at 3 and 6 months
The change in the mean early diastolic mitral annular velocity (mean e'), at 3 and 6 months
adverse drug effects
adverse drugs effects
Change in N-terminal pro-BNP (NT-proBNP)
Change in N-terminal pro-BNP (NT-proBNP)
Neutrophil/lymphocyte ratio -AMPK pathway
Neutrophil/lymphocyte ratio -AMPK pathway
Inflammatory and oxidative stress
Inflammatory and oxidative stress
Change in body weight
Change in body weight

Full Information

First Posted
October 8, 2023
Last Updated
October 8, 2023
Sponsor
October University for Modern Sciences and Arts
Collaborators
clinical research unit, El-sheikh zayed specialized hospital - Egyptian Ministry of health
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1. Study Identification

Unique Protocol Identification Number
NCT06080802
Brief Title
The Effect of Addition of Metformin to SGLT2 In Diabetic Patients With Heart Failure With Preserved Ejection Fraction
Official Title
The Effect of Addition of Metformin to SGLT2 In Diabetic Patients With Heart Failure With Preserved Ejection Fraction
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 1, 2023 (Anticipated)
Primary Completion Date
November 1, 2024 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
October University for Modern Sciences and Arts
Collaborators
clinical research unit, El-sheikh zayed specialized hospital - Egyptian Ministry of health

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
Yes

5. Study Description

Brief Summary
a prospective open-label, randomized controlled study to evaluate the efficacy of the addition of metformin to SGLT2 in diabetic patient with preserved ejection fraction
Detailed Description
Regardless of the benefits noted with SGLT2is, metformin is recommended as first-line therapy for glycemic control in individuals with T2DM and HF, including HFpEF, with estimated glomerular filtration rates (eGFRs) ≥30 mL/min/1.73 m2. This is based on the demonstrated experience with long-term use; its safety, low cost, and low side effect profile; as well as observational (not clinical trial) data suggesting a 20% relative risk reduction in mortality in individuals with HF, including HFpEF. Nevertheless, it is worth mentioning that Metformin is a common anti-diabetic drug with both systemic and cardioprotective benefits in addition to its hypoglycaemic effect. At the cellular level metformin activates adenosine monophosphate-activated protein kinase (AMPK) an important regulator of several metabolic pathways resulting in enhanced glucose utilisation, reduction of protein synthesis and improvement of mitochondrial function. Furthermore, metformin has been shown to reduce collagen accumulation and potentially reduce LV hypertrophy and improve diastolic function in the diabetic myocardium. The cardio protection afforded by metformin treatment seems to result from interference with TGF-beta signaling pathway and activation of the AMP-kinase signaling cascade. A recent systematic review and meta regression analysis have shown that metformin treatment was associated with a reduction in mortality in patients with HFpEF. In addition, treatment with metformin of non-diabetic metabolic syndrome patients with diastolic dysfunction, on top of lifestyle counseling, was associated with improved diastolic function. Nevertheless, a recent met analysis showed that initial SGLT2 inhibitor/metformin combination therapy has glycaemic and weight benefits compared with either agent alone and appears relatively safe. High dose SGLT2 inhibitor/metformin combination therapy appears to have modest weight, but no glycaemic benefits compared with the low dose combination therapy. based on that we our aim is to evaluate the efficacy of the addition of metformin to SGLT2 in diabetic patient with preserved ejection fraction

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure With Preserved Ejection Fraction, Diabete Type 2
Keywords
metformin, SGLTi, HFpEF

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
control(SGLT2i/ARBs/MRA/ +/- diuretics).
Arm Type
No Intervention
Arm Description
Lifestyle counseling plus standard evidence-based therapy for HFpEF (SGLT2i/ARBs/MRA/ +/- diuretics).
Arm Title
intervention
Arm Type
Experimental
Arm Description
Lifestyle counseling plus standard evidence-based therapy for HFpEF (SGLT2i/ARBs/MRA/ +/- diuretics)+ metformin
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
The intervention will consist in giving metformin starting with 500 mg once daily 1 gm daily (at breakfast) during the first week; if well tolerated, the dose was progressively increased to 500 mg twice daily (at breakfast and dinner) during week 2, to 1000 mg at breakfast and 500 mg at dinner during week 3, in order to reach the target dose of 1000 mg twice daily (at breakfast and dinner) during the rest of the follow-up. Patients will be followed up by telephone call 2 weeks intervals during the study period 5 SGL-2 will be prescribed to group 1 after diagnosis with HFpEF while group 2 will have SGL-2 and Metformin
Primary Outcome Measure Information:
Title
Hospitalization rate
Description
Hospitalization rate
Time Frame
baseline, 3 and 6 months
Title
HRQOL using Minnesota Living with Heart Failure Questionnaire for quality-of-life evaluation (MLFHQ)
Description
HRQOL using Minnesota Living with Heart Failure Questionnaire for quality-of-life evaluation (MLFHQ)
Time Frame
baseline, 3 and 6 months
Secondary Outcome Measure Information:
Title
The change in the mean early diastolic mitral annular velocity (mean e'), at 3 and 6 months
Description
The change in the mean early diastolic mitral annular velocity (mean e'), at 3 and 6 months
Time Frame
baseline, 3 and 6 months
Title
adverse drug effects
Description
adverse drugs effects
Time Frame
baseline, 3 and 6 months
Title
Change in N-terminal pro-BNP (NT-proBNP)
Description
Change in N-terminal pro-BNP (NT-proBNP)
Time Frame
baseline, 3 and 6 months
Title
Neutrophil/lymphocyte ratio -AMPK pathway
Description
Neutrophil/lymphocyte ratio -AMPK pathway
Time Frame
baseline, 3 and 6 months
Title
Inflammatory and oxidative stress
Description
Inflammatory and oxidative stress
Time Frame
baseline, 3 and 6 months
Title
Change in body weight
Description
Change in body weight
Time Frame
baseline, 3 , 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age of 40 years to 74 years. HFpEF (≥ 50%) Written informed consent of the subject to participate in the study. New York Heart Association functional class I-IV. Diabetic patients SGL-2 naive. Newly diagnosed heart failure of preserved ejection fraction Exclusion Criteria: Patients with heart failure with reduced ejection fraction (< 40%) Age less than 40 and more than 74 GFR < 30 mL/min A1c > 9 Known allergy to metformin End- stage liver disease Cancer Pregnancy or lactation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
sara M eladawy
Phone
01222124567
Email
smeladway@msa.edu.eg
First Name & Middle Initial & Last Name or Official Title & Degree
hassan abdellatif
Phone
01092990402
Email
hassangamal79@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
sara M eladawy
Organizational Affiliation
MSA university
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Mai abdelhafez, PhD
Organizational Affiliation
MSA university
Official's Role
Study Chair
Facility Information:
Facility Name
clinical research uint- El-sheikh zayed specialized hospital SMC- Egyptian Ministry of health
City
Cairo
Country
Egypt
Facility Contact:
First Name & Middle Initial & Last Name & Degree
hassan abdellatif
Phone
01092990402
Email
hassangamal79@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36507650
Citation
ElSayed NA, Aleppo G, Aroda VR, Bannuru RR, Brown FM, Bruemmer D, Collins BS, Hilliard ME, Isaacs D, Johnson EL, Kahan S, Khunti K, Leon J, Lyons SK, Perry ML, Prahalad P, Pratley RE, Seley JJ, Stanton RC, Gabbay RA, on behalf of the American Diabetes Association. 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Care in Diabetes-2023. Diabetes Care. 2023 Jan 1;46(Suppl 1):S140-S157. doi: 10.2337/dc23-S009.
Results Reference
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PubMed Identifier
37137593
Citation
Kittleson MM, Panjrath GS, Amancherla K, Davis LL, Deswal A, Dixon DL, Januzzi JL Jr, Yancy CW. 2023 ACC Expert Consensus Decision Pathway on Management of Heart Failure With Preserved Ejection Fraction: A Report of the American College of Cardiology Solution Set Oversight Committee. J Am Coll Cardiol. 2023 May 9;81(18):1835-1878. doi: 10.1016/j.jacc.2023.03.393. Epub 2023 Apr 19. No abstract available.
Results Reference
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The Effect of Addition of Metformin to SGLT2 In Diabetic Patients With Heart Failure With Preserved Ejection Fraction

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