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Evaluation of effects of aqueous extract of Iranian oak (Quercus brantii) on antioxidant capacity and stress oxidative of thalassemia patients

Evaluation of effects of aqueous extract of Iranian oak (Quercus brantii) on antioxidant capacity and stress oxidative of thalassemia patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016040427205N1
Enrollment
90
Registered
2016-06-27
Start date
2016-04-03
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

Thalassaemia. Beta thalassaemia

Interventions

Intervention 1: Intervention group : Patients with thalassemia major will receive two capsules daily for four months each capsule contains 150 mg extract oak. Intervention 2: Control group: thalassem
Treatment - Drugs
Placebo
Intervention group : Patients with thalassemia major will receive two capsules daily for four months each capsule contains 150 mg extract oak
Control group: thalassemia Patients in the control group will receive two placebo capsule daily for four months.

Sponsors

Sharekord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Patients with thalassemia major 2. patients with regular blood transfusions 3. Patients who received chelation therapy (desferal) at least four days a week 4. 10-60 years old 5. getting informed consent Exclusion criteria: 1. Under 10 years 2. Positive Hepatitis 3. Positive HIV   4. heart failure and chronic kidney disease 5. peregnance 6. chelating not answer or other chelating use.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Ferritin. Timepoint: Before and after of study. Method of measurement: ELIZA.;Iron. Timepoint: Before and after of study. Method of measurement: Biochemical Auto analizer.;Glutathione peroxidase. Timepoint: Before and after of study. Method of measurement: Spectrophotometric.;Catalase. Timepoint: Before and after of study. Method of measurement: Spectrophotometric.;Superoxide dismutase. Timepoint: Before and after of study. Method of measurement: Spectrophotometric.;Carbonyl protein. Timepoint: Before and after of study. Method of measurement: Spectrophotometric.;Malondialdehyde. Timepoint: Before and after of study. Method of measurement: HPLC.;Total Capacity Antioxidant. Timepoint: Before and after of study. Method of measurement: Spectrophotometric.

Secondary

MeasureTime frame
Alanin Transferase. Timepoint: Before and after of study. Method of measurement: Biochemical auto analyzer.;Aspartate amino transferase. Timepoint: Before and after of study. Method of measurement: Biochemical auto analyzer.;Triglyceride. Timepoint: Before and after of study. Method of measurement: Biochemical auto analyzer.;Cholestrol. Timepoint: Before and after of study. Method of measurement: Biochemical auto analyzer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdi Babamir

Sharekord University of Medical Science

Mahdibabamir@yahoo.com+98 38 3444 4445

Outcome results

None listed

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