Efficacy of Metformin as add-on Therapy in Non-Diabetic Heart Failure Patients

Sponsor
Cairo University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05177588
Collaborator
(none)
80
1
2
18
4.5

Study Details

Study Description

Brief Summary

There is an increasing interest in the use of metformin in CV diseases and there is an increasing interest in studying its potential new roles in heart failure patients. There were some concerns related to the safety of metformin in such diabetic patients due to the risk of lactic acidosis. However, recent studies showed that metformin was safe or even beneficial in HF patients. We hypothesized that metformin might improve morbidity, mortality, cardiac function, and HR-QoL in non-diabetic patients with HFrEF.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Metformin is an anti-diabetic drug that is known improve insulin sensitivity and reduce insulin resistance. A published meta-analysis of randomized controlled trials (RCTs) reported a reduction of weight and insulin resistance in metformin users. Animal models also showed that metformin reduces cardiac hypertrophy. Observational studies showed a beneficial effect for metformin in patients with type 2 diabetes mellitus (T2DM) and heart failure. A recent study found that metformin reduced oxidative stress in non-diabetic patients with CAD.

Metformin has multiple modes of actions involving both AMP-activated protein kinase (AMPK) dependent and AMPK-independent mechanisms that may be implicated in cardiac hypertrophy. At the systemic level, a review of clinical and experimental data showed that metformin improves endothelial function, protects from oxidative stress and inflammation, as well as the negative effects of angiotensin II. Observational studies also reported cardiovascular benefits in metformin users especially in patients with type 2 diabetes mellitus (T2DM) and heart failure. Metformin has also been shown to exert a cardio protective effect and it has been shown to reduce oxidative stress which is a common finding in heart failure patients. For these reasons, there is an increasing interest in the use of metformin in CV diseases and there is an increasing interest in studying its potential new roles in this aspect. We hypothesized that metformin might improve morbidity, mortality, cardiac function, and HR-QoL in non-diabetic patients with HFrEF.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This is a prospective, interventional, randomized controlled, open label study. The study sample will include heart failure patients with pre-diabetesThis is a prospective, interventional, randomized controlled, open label study. The study sample will include heart failure patients with pre-diabetes
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Efficacy of Metformin as add-on Therapy in Non-Diabetic Heart Failure Patients
Actual Study Start Date :
Jul 1, 2021
Anticipated Primary Completion Date :
Dec 30, 2022
Anticipated Study Completion Date :
Dec 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Metformin

Patients in the metformin group will receive a starting dose of 1000 mg/day. The dose will be titrated as tolerated to a maximum of 2000 mg/. Patients will receive the medications for six year and will be followed up for the duration of the study. Patients will be assessed at baseline, 3 months, and 6 months.

Drug: Metformin
Metformin 2000 mg/day

No Intervention: Standard of Care

Patients in the control arm will continue the SOC medications

Outcome Measures

Primary Outcome Measures

  1. Left ventricular mass index [6 months]

    The regression of left ventricular mass (LVM) as assessed by echocardiography

  2. Ejection Fraction [6 months]

    Ejection fraction as assessed by echocardiography

Secondary Outcome Measures

  1. Total antioxidant capacity [3 and 6 months]

  2. Malondialdehyde (MDA) or TBARS [3 and 6 months]

  3. Health related quality of life [3 and 6 months]

    HR-QoL as assessed by Minnesota living with heart failure questionnaire (MLFHQ)

  4. New York Heart Association functional classification (NYHA): [3 and 6 months]

    The NYHA classifies patients in one of four possible categories based on the physical activity limitations; the limitations/symptoms are in regards to normal breathing andvarying degrees in shortness of breath and or angina pain

  5. Hospitalization rate [3 and 6 months]

    The number of hospitalizations within each group will be calculated during the study period

  6. Adverse reactions of metformin [3 and 6 months]

    Incidence of lactic acidosis

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 79 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Chronic heart failure (>6 months duration)

  • Stabilized on recommended or maximally tolerated dose of ACE-I/ARB (unless contraindicated) and beta-blocker (unless contraindicated). If indicated, an aldosterone receptor antagonist should be given (unless contraindicated).

  • Reduced ejection fraction defined as LVEF < 40%

  • NYHA-class II or III or IV with stable symptoms for at least the past 3 months

  • Creatinine clearance > 45 ml/min

Exclusion Criteria:
  • Diabetes mellitus: Diabetes will be diagnosed using the 2018 The American Diabetes Association (ADA) "Standards of Medical Care in Diabetes 15

  • FPG ≥126 mg/dL (7.0 mmol/L). Fasting is defined as no caloric intake for at least 8 h.*

  • 2-h PG ≥200 mg/dL (11.1 mmol/L) during OGTT. The test should be performed as described by the WHO, using a glucose load containing the equivalent of 75-g anhydrous glucose dissolved in water.

  • A1C ≥6.5% (48 mmol/mol). The test should be performed in a laboratory using a method that is NGSP certified and standardized to the DCCT assay.*

  • In a patient with classic symptoms of hyperglycemia or hyperglycemic crisis, a random plasma glucose ≥200 mg/dL (11.1 mmol/L).

  • Any oral or injectable hypoglycemic therapy (e.g. insulin, sulfonylureas)

  • Recent Hospitalizations in the past 3 months

  • Metformin treatment within the last 3 months

  • Creatinine clearance below 45 in the prior 6 months as assessed by Cockcroft and Gault equation

  • Known allergy to metformin or major side effects to metformin treatment

  • Atrial fibrillation with poorly controlled ventricular rate at rest (> 100 beats/min)

  • Hypertrophic cardiomyopathy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Agouza Hospital Giza Egypt 12566

Sponsors and Collaborators

  • Cairo University

Investigators

  • Principal Investigator: Ahmed M Kamel, MSc., Faculty of Pharmacy, Cairo University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ahmed Mohamed Sayed Kamel, Mr., Cairo University
ClinicalTrials.gov Identifier:
NCT05177588
Other Study ID Numbers:
  • CL (2582)
First Posted:
Jan 4, 2022
Last Update Posted:
Jan 4, 2022
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
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
Keywords provided by Ahmed Mohamed Sayed Kamel, Mr., Cairo University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 4, 2022