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Evaluation of the efficacy of defroxamine- deferiprone on cardiac function in patients with thalassemia major

Clinical trial in evaluation of the efficacy of defroxamine-deferiprone on cardiac function in patients with major thalassemia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014070512765N4
Enrollment
12
Registered
2014-08-08
Start date
2010-02-23
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

Thalassemia major. Beta thalassemia major

Interventions

Treatment by Deferiprone with a dose of 50-100 mg/kg daily associated with treatment by Deferoxamine with a dose of 50-30 mg/kg for 3 nights weekly.
Treatment - Drugs
Treatment by Deferiprone with a dose of 50-100 mg/kg daily associated with treatment by Deferoxamine with a dose of 50-30 mg/kg for 3 nights weekly

Sponsors

Golestan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients were treated with iron chelators Subcutaneous Deferoxamine with a doseof 30-50 mg/kg for 5 nights a week for 3 years before starting the study. Exclusion criteria: gastrointestinal complications; failure to cooperate in the control tests (ALT, CBC); becoming tired of the traffic for controlling consumption of deferiprone

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Left Venticular Ejection Fraction. Timepoint: It is messured for 3 years at the end of each year. Method of measurement: Echocardiography.;Srum ferritin. Timepoint: It is messured for 3 years at the end of each year. Method of measurement: Determining the level of serum ferritin by related test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNarges beigom Mirbehbahani

Hematology & Oncology Research Center, Golestan University of Medical Sciences

n.mirbehbahani@gmail.com+98 17 1232 8539

Outcome results

None listed

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