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Quercetin on thalassemia induced depression

Study of the effect of oral quercetin supplement intake on mood in ß-thalassemia major patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20091114002709N46
Enrollment
84
Registered
2018-02-11
Start date
2017-04-22
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

beta thalassemia major. Cooley anaemia Severe beta thalassaemia Thalassaemia: intermedia major

Interventions

Intervention 1: Intervention group: a group of 42 thalassemia patients recieved quercetin tablets.They consumed one tablet containing 500 mg quercetin after lunch every day for 3 months and they were

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 18 to 40 year old male and female beta thalassemia major patients Inclination to cooperate and signing the written informed consent A minimum of 2 years of blood transfusion history blood specimen collection 20 days after the last blood transfusion Regular and peculiar iron-chelating therapy with desferrioxamine Vitamin C supplement intake with desferrioxamine

Exclusion criteria

Exclusion criteria: Uncontrollable and life threatening complication due to due to the supplement intake;; ; ; ; ; ; A change in type or amount of the iron chelator Pregnancy or lactation Hepatitis infection and other metabolic or infectious diseases Less than 80% compliance of supplement intake Consumption of drugs that interfere with quercetin Drinking more than 500 mg/day of beverages rich in flavonoids Smoking or alcohol consumption

Design outcomes

Primary

MeasureTime frame
Depression. Timepoint: before and after the intervention. Method of measurement: Beck's questionnaire.

Secondary

MeasureTime frame
High-sensitivity C-reactive protein(hs-CRP). Timepoint: before and after the intervention. Method of measurement: using ELISA kit in Microgram/milliliter(micg/ml).;Tumor necrosis factor a(TNF-a). Timepoint: before and after the intervention. Method of measurement: using ELISA kit in Picrogram/milliliter(pg/ml).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Azita Azarkeivan

Blood Transfusion Education & Research Institute.

azazarkeivan@yahoo.com+98 21 8800 9222

Outcome results

None listed

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