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Effect of Imatinib Mesylate in patients undergone allogeneic bone marrow transplantation who show chronic coetaneous involvement Graft Versus-Host Disease.

Phase 2
Conditions
cutaneous cGVHD.
Graft-versus-host reaction or disease
Registration Number
IRCT201302261030N12
Lead Sponsor
Hematology-Oncology and SCT Research Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
28
Inclusion Criteria

Inclusion Criteria
1- The patient shall undergo allogen bone marrow transplantation and have clinical and pathological cutaneous CGVHD criteria.
2- Patient’s cutaneous signs are not improved by taking corticosteroids with doses of 0.5 mg/kg at least for 3 months and cyclosporine.
3- The cutaneous signs shall be active.
4- The patient shall be aged between 16 to 60 years old.
Exclusion Criteria
1- Pregnancy
2- Having a history of taking Rituximab.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The extent of cutaneous involvment. Timepoint: At the start of treatment and in the end of 6 month. Method of measurement: Skin examination.
Secondary Outcome Measures
NameTimeMethod
Extent of skin involvement in pathology. Timepoint: At the start of treatment and in the end of 6 month. Method of measurement: Severity of involvement in pathology.;Side effect frequency. Timepoint: Every month after treatment up to 6 months. Method of measurement: Examination and fallowing treatment.
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