Skip to content

Quercetin in thalassemia

The effect of oral quercetin supplement intake on oxidative markers , serum iron, liver enzymes and inflammatory indices in ß-thalassemia major patients,a double-blind placebo-controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201701172709N43
Enrollment
84
Registered
2017-04-13
Start date
2017-03-21
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

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

Interventions

Intervention 1: quercetin,90 tablets,500mg,3 months, once a day after a meal. Intervention 2: starch placebo, 90 tablets,500 mg, 3 months, once a day after a meal.
Treatment - Drugs
Placebo
quercetin,90 tablets,500mg,3 months, once a day after a meal
starch placebo, 90 tablets,500 mg, 3 months, once a day after a meal

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 18 to 30 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; Serum ferritin level between 2500 to 3500 ng/ml 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; Splenectomy; 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

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Malone dialdehyde (MDA). Timepoint: before and after the intervention. Method of measurement: nmol/gHb, colorimetry.;Total antioxidant capacity (TAC). Timepoint: before and after the intervention. Method of measurement: mmol/L, colorimetry.;Superoxide dismutase (SOD). Timepoint: before and after the intervention. Method of measurement: U/gHb, colorimetry.;Glutathione peroxidase (GPx). Timepoint: before and after the intervention. Method of measurement: U/gHb, colorimetry.

Secondary

MeasureTime frame
Serum Fe. Timepoint: before and after the intervention. Method of measurement: spectrophotometry,µg/dl.;Serum transferrin. Timepoint: before and after the intervention. Method of measurement: immunoturbidometry, mg/dl.;Serum ferritin. Timepoint: before and after the intervention. Method of measurement: spectrophotometry, ng/ml.;Total antioxidant capacity (TIBC). Timepoint: before and after the intervention. Method of measurement: calorimetry, µg/dl.;Transferrin saturation. Timepoint: before and after the intervention. Method of measurement: formula, %.;Aspartate transaminase (AST). Timepoint: before and after the intervention. Method of measurement: enzymatic calorimetry, IU/L.;Alanin transaminase (ALT). Timepoint: before and after the intervention. Method of measurement: enzymatic calorimetry, IU/L.;Alkaline phosphatase (ALP). Timepoint: before and after the intervention. Method of measurement: enzymatic calorimetry, IU/L.;High-sensitivity C reactive protein (hs-CRP). Timepoint: before and after the intervention. Method of measurement: ELISA, µg/ml.;Tumor necrosis factor alpha (TNF). Timepoint: before and after the intervention. Method of measurement: Elisa, pg/ml.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Azita Azarkeivan

High Institute for Research and Education in Transfusion Medicine

azazarkeivan@yahoo.com+98 22920088

Outcome results

None listed

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