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The effect of hesperidin in myocardial infarction

Effect of hesperidin supplementation on depressive symptoms, serum levels of BDNF and cortisol in patients after myocardial infarction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201702262394N36
Enrollment
70
Registered
2017-04-26
Start date
2017-05-05
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Depression. Depressive episode

Interventions

Intervention 1: Intervention group: supplements of hesperidin, capsules 200 mg orally, once a day for three months. Intervention 2: Control group: placebo containing starch, 200 mg capsules orally, on
Treatment - Drugs
Placebo
Intervention group: supplements of hesperidin, capsules 200 mg orally, once a day for three months
Control group: placebo containing starch, 200 mg capsules orally, once a day for three months

Sponsors

Vice chancellor for research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: willingness to cooperate and signed informed consent; Do not use any supplements during the last 3 months; including omega-3, 10 Q, antioxidants and vitamins; The absence of any allergies (gastrointestinal and skin) to any type of antioxidant supplements and vitamins, age 30 to 70 years; Beck Depression Inventory score more than 10; patients with MI from discharge to 6 weeks after MI; Do not use more than one blood orange or Do not use more than two other citrus fruits a day; BMI=25-40. Criteria of excluding: There are major psychiatric disorders in patients with history; treatment of depression over 1 year ago; taking more than 500 ml per day of flavonoid-rich beverages include tea, coffee, citrus juice; Major cognitive disorders or impaired cognitive function of the patient's history; Lack of follow-up after discharge; Smoking and tobacco; uncontrolled development of metabolic diseases; Pregnancy and lactation; Use heparin and warfarin. Exclusion criteria: The use of any antioxidant and vitamin supplements; View the latest allergy symptoms at any time during the study; unwillingness to continue the cooperation of the patient for any reason; uncontrolled chronic diseases ( Like: hepatic failure, renal failure, diabetes, etc.); digestive disorders; compliance below 80%; Earn each of the criteria of entry.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression. Timepoint: Before the intervention, after the intervention. Method of measurement: Beck standard questionnaire.

Secondary

MeasureTime frame
Brain-Derived Neurotrophic Factor. Timepoint: Before the intervention, after the intervention. Method of measurement: ng per ml in the ELISA.;Cortisol. Timepoint: Before the intervention, after the intervention. Method of measurement: micrograms per deciliter, ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Reza Vafa

Vice chancellor for research, Iran University of Medical Sciences

rezavafa@yahoo.com+98 21 8670 4805

Outcome results

None listed

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