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Completed

NCT Number: NCT06056687

Alpha-lipoic Acid in Diabetic Patients With Ischemic Cardiomyopathy

The aim of this study is to investigate the effect of alpha-lipoic acid on inflammatory markers and cardiac fibrosis markers in diabetic patients with Ischemic Cardiomyopathy.

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Key information

Age range

20 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Damanhour Teaching Hospital, General Organization for Teaching Hospitals and Institutes.

Damanhūr, Elbehairah, 31527, Egypt

About this study

  • A 3-month, prospective double blind interventional study, which will include 60 patients with type II Diabetes Mellitus with Ischemic Cardiomyopathy on optimal standard medical therapy, who will be consecutively randomized into two groups, group on ALA 600 mg once daily and the second group on placebo once daily.
  • Approval will be obtained from Research and Ethics Committee of Faculty of Pharmacy, Damanhour University. A written informed consent will be obtained from patients before begining of the study.
  • All patients will undergo complete physical examination at baseline and after 3 months of treatment.
  • Patients will be assessed using Echocardiography before and after the study focusing on:

Left atrial diameter (LAD), basic left ventricular dimensions (EDD and ESD) and both systolic and diastolic function.

-Measurements of inflammatory markers such as [C-reactive protein (CRP), Tumor necrosis factor alpha (TNFα)] and fibrosis markers such as [Transforming growth factor beta (TGFβ), Matrix metalloproteinase 2 (MMP-2)] at the beginning of the study and after 3 months of the study.

Study Outcomes: all patients will be followed up for 3 months for:

  • 1ry outcomes: Change in inflammatory and fibrosis markers levels. LV Echocardiography improvements of any of basic Echo parameters.
  • 2ry outcomes: Major Adverse Cardiovascular Events (MACE) such as MI, stroke or death. any side effects of the drug. Results The results of the study will be tabulated and statistical tests appropriate to the study will be conducted to evaluate significance of results.

conclusion Conclusion, and recommendations will be given.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Type 2 diabetes with a history of CAD.
  • LV ejection fraction (LVEF) ≤40%.
  • Ischemic heart failure patients with NYHA grade II-IV.

Exclusion criteria

  • Type 1 diabetes.
  • Severe CKD with GFR ≤ 15 ml/min/1.73m^2.
  • Severe liver disease.
  • Thyroid disorders.
  • Acute febrile illness.
  • Autoimmune disorders or connective tissue disorders.

Treatment and study plan

Alpha Lipoic Acid 600 MG Oral Tablet

Drug

Alpha Lipoic Acid 600 MG Oral Tablet once daily

Other names: Thiotacid 600 mg

Placebo tablet

Other

Placebo Tablet once daily

Other names: Placebo

Primary outcomes

  1. C-reactive protein (CRP)

    Time frame: 3 month

    Serum Biomarker (mg/ml)

  2. Tumor necrosis factor alpha (TNFα)]

    Time frame: 3 Months

    Serum Biomarker (pg/ml)

  3. Transforming growth factor beta (TGFβ)

    Time frame: 3 Months

    fibrosis markers (ng/ml)

  4. Matrix metalloproteinase 2 (MMP-2)

    Time frame: 3 Months

    fibrosis markers (ng/ml)

Sponsors and collaborators

Lead sponsor

Damanhour University

Other

Registry information

Official study title

Effect of Alpha-lipoic Acid on Inflammatory and Cardiac Fibrosis Markers in Diabetic Patients With Ischemic Cardiomyopathy

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Sep 28, 2023
Registry last updated
Feb 21, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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