Clinical Trials Directory

Trials / Completed

CompletedNCT06468423

Comparison of Deferasirox and Desferoxamine in Patients of β-Thalassemia Major With Iron Overload

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
142 (actual)
Sponsor
RESnTEC, Institute of Research · Academic / Other
Sex
All
Age
2 Years – 15 Years
Healthy volunteers
Not accepted

Summary

This study was planned to compare deferasirox and desferrioxamine in terms of mean serum ferritin levels in patients of β-thalassemia major having Iron overload. Choosing an effective iron chelator is crucial to increasing iron chelation therapy compliance. Not much local data exists in Pakistan comparing the effectiveness of deferasirox (DFX) and desferrioxamine (DFO), so, this study would be helpful in providing baseline data and formulating new protocols for iron chelation therapy, in which DFX may be a useful oral alternative to parenteral DFO.

Conditions

Interventions

TypeNameDescription
DRUGDeferasirox (DFX)Oral DFX at a dose of 30mg/kg daily advised for a duration of 6 months.
DRUGDeferoxamine (DFO)DFO group (n=71) included children who were given DFO at a dose of 50 mg/kg through the subcutaneous route by infusion pump five days a week for a duration of 6 months.

Timeline

Start date
2023-01-01
Primary completion
2023-09-30
Completion
2023-09-30
First posted
2024-06-21
Last updated
2024-06-21

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06468423. Inclusion in this directory is not an endorsement.