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Effect of exjade on level in patients with thalassemia

Comparative study of the efficacy of combination and single therapy of exjade and desferal on ferritin level in patients with major thalassemia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201412097677N3
Enrollment
90
Registered
2015-06-07
Start date
2014-05-22
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

major thalassemia. Beta thalassaemia

Interventions

Intervention 1: Intervention group1: Exjade
Novartis plant in France
tablets 20 mg per kg body weight
3 times a day for 6 months. Intervention 2: Intervention group2: Deferoxamine and Exjade
Deferoxamine subcutaneous 40 mg per kg of body weight and tablet Exjade dose of 10 mg per kg of body weight
Deferoxamine once a two days and tablet Exjade once a day for 6 month. Intervention 3: Control group:Deferoxamine
subcutaneous 40 mg per kg body weight
once daily for 6 months.
Treatment - Drugs
Intervention group1: Exjade
3 times a day for 6 months
Intervention group2: Deferoxamine and Exjade

Sponsors

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

Eligibility

Sex/Gender
All
Age
No minimum to 14 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Approved based on clinical symptoms and history of thalassemia and hemoglobin electrophoresis; full cooperation during the study; treatment with deferoxamine subcutaneous injection and ferritin levels below 3000. Exclusion criteria: Deferiprone gastrointestinal intolerance; leukocytes less than 3,000; severe liver disease; ascites; lack of consent, lack of cooperation in the history of previous treatment regimens (blood transfusion and deferoxamine).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Serum ferritin level. Timepoint: Before the intervention; three months after the intervention and six months after intervention. Method of measurement: Based on the results of test ferritin.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Akramipour

Kermanshah university of medical sciences

Akramipur20@yahoo.com+98 83 3721 8202

Outcome results

None listed

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