C92.0 C91.0 T86.0 B25.9
Conditions
Interventions
Group 1: Non-interventional. Regular follow up according to guidelines. Data collection. The aim of the study is the prospective validation of transplant risk models that have been developed using dif
Sponsors
Universitätsklinikum Essen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: First allogeneic HCT
Exclusion criteria
Exclusion criteria: Second or further allogeneic HCT, Hemoglobinopathies.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall survival | — |
Secondary
| Measure | Time frame |
|---|---|
| Cytomegalovirus reactivation within first 100 days from HCT | — |
Countries
Germany
Contacts
Public ContactAmin Turki
Universitätsklinikum Essen
Outcome results
None listed