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The effect of Lycopene on the expression level of Mir-210, Antioxidant factors and apolipoproteins in patients with ischemic heart failure referring to Isfahan Chamran hospital: A randomized Clinical Trial

The effect of Lycopene on the expression level of Mir-210, Antioxidant factors and apolipoproteins in patients with ischemic heart failure referring to Isfahan Chamran hospital: A randomized Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200914048711N1
Enrollment
48
Registered
2024-03-03
Start date
2024-03-10
Completion date
Unknown
Last updated
2024-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congestive heart failure. Heart failure

Interventions

Intervention 1: Intervention group: Lycopene, one 25 mg tablet daily, for 60 days, 21st Century company, made in USA, contains 25 mg of lycopene and 170 mg of calcium carbonate. Intervention 2: Contro

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with ischemic heart failure Age: 40 -70 years olds Ejection Fraction: 20 - 40

Exclusion criteria

Exclusion criteria: Patients with cancer, nephrotic diseases, diabetes, autoimmune diseases, organ transplantation, immunosuppressive drugs, bronchial diseases, stroke, arrhythmia, late surgery, active viral infection, active internal hemorrage, anemia with Hb<10g/dl Smoking

Design outcomes

Primary

MeasureTime frame
Heart function. Timepoint: Before of intervention, 60 days after of intervention. Method of measurement: Echocardiogram.;Lipid profile. Timepoint: Before of intervention, 60 days after of intervention. Method of measurement: Auto analyzer biochemistry.;Total antioxidant capacity. Timepoint: Before of intervention, 60 days after of intervention. Method of measurement: Assay kit, Spectrophotometer.;Paraoxonase enzyme activity assay. Timepoint: Before of intervention, 60 days after of intervention. Method of measurement: Assay kit, Spectrophotometer.;Arylesterase enzyme activity assay. Timepoint: Before of intervention, 60 days after of intervention. Method of measurement: Assay kit, Spectrophotometer.;LDL separation from plasma. Timepoint: Before of intervention, 60 days after of intervention. Method of measurement: Ultracentrifuge.;Assessment of LDL oxidation. Timepoint: Before of intervention, 60 days after of intervention. Method of measurement: Cuso4, Spectrophotometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLaila Rejali

Islamic Azad University

lailarejali@yahoo.com+98 31 3742 0134

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026