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Alpha-lipoic Acid in Diabetic Patients With Ischemic Cardiomyopathy

Primary Purpose

Ischemic Cardiomyopathy, Diabetes Mellitus

Status
Recruiting
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Alpha Lipoic Acid 600 MG Oral Tablet
Placebo Tablet
Sponsored by
Damanhour University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Cardiomyopathy

Eligibility Criteria

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

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.

Sites / Locations

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

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Alpha Lipoic Acid Group

Placebo Group

Arm Description

ALA 600 mg once daily

the second group on placebo once daily

Outcomes

Primary Outcome Measures

C-reactive protein (CRP)
Serum Biomarker (mg/ml)
Tumor necrosis factor alpha (TNFα)]
Serum Biomarker (pg/ml)
Transforming growth factor beta (TGFβ)
fibrosis markers (ng/ml)
Matrix metalloproteinase 2 (MMP-2)
fibrosis markers (ng/ml)

Secondary Outcome Measures

Full Information

First Posted
September 21, 2023
Last Updated
September 26, 2023
Sponsor
Damanhour University
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1. Study Identification

Unique Protocol Identification Number
NCT06056687
Brief Title
Alpha-lipoic Acid in Diabetic Patients With Ischemic Cardiomyopathy
Official Title
Effect of Alpha-lipoic Acid on Inflammatory and Cardiac Fibrosis Markers in Diabetic Patients With Ischemic Cardiomyopathy
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2023 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
January 1, 2024 (Anticipated)

3. Sponsor/Collaborators

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

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Cardiomyopathy, Diabetes Mellitus

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
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.
Masking
ParticipantInvestigator
Masking Description
Double Blind
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Alpha Lipoic Acid Group
Arm Type
Experimental
Arm Description
ALA 600 mg once daily
Arm Title
Placebo Group
Arm Type
Placebo Comparator
Arm Description
the second group on placebo once daily
Intervention Type
Drug
Intervention Name(s)
Alpha Lipoic Acid 600 MG Oral Tablet
Other Intervention Name(s)
Thiotacid 600 mg
Intervention Description
Alpha Lipoic Acid 600 MG Oral Tablet once daily
Intervention Type
Other
Intervention Name(s)
Placebo Tablet
Other Intervention Name(s)
Placebo
Intervention Description
Placebo Tablet once daily
Primary Outcome Measure Information:
Title
C-reactive protein (CRP)
Description
Serum Biomarker (mg/ml)
Time Frame
3 month
Title
Tumor necrosis factor alpha (TNFα)]
Description
Serum Biomarker (pg/ml)
Time Frame
3 Months
Title
Transforming growth factor beta (TGFβ)
Description
fibrosis markers (ng/ml)
Time Frame
3 Months
Title
Matrix metalloproteinase 2 (MMP-2)
Description
fibrosis markers (ng/ml)
Time Frame
3 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rehab H Werida, Ass. Prof.
Phone
+201005359968
Email
rehabwrieda@pharm.dmu.edu.eg
First Name & Middle Initial & Last Name or Official Title & Degree
Aya Shama, Bachlor
Email
a.shama22566@pharm.dmu.edu.eg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rehab H Werida, Ass Prof.
Organizational Affiliation
Damanhour University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Noha El bassiouny, Lecturer
Organizational Affiliation
Damanhour University
Official's Role
Study Director
Facility Information:
Facility Name
Damanhour Teaching Hospital, General Organization for Teaching Hospitals and Institutes.
City
Damanhūr
State/Province
Elbehairah
ZIP/Postal Code
31527
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rehab H Werida, Ass. Prof.
Phone
01005359968
Email
rehabwrieda@pharm.dmu.edu.eg
First Name & Middle Initial & Last Name & Degree
Aya Shama, Bachlor
Phone
01558515369
Email
a.shama22566@pharm.dmu.edu.eg

12. IPD Sharing Statement

Learn more about this trial

Alpha-lipoic Acid in Diabetic Patients With Ischemic Cardiomyopathy

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