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Clinical Trial Summary

Register of patients with blood stem cell transplantations (autologous, allogen).


Clinical Trial Description

Documenting the success rate in terms of complication rate, disease response, survival rate, engraftment, and details of transplantation settings, for example donor and conditioning data, remission status before transplantation. It's a register of patients who have one or more autologous and / or allogenic blood stem cell transplants due to an existing indication for performing myeloablative / non-myeloablative high-dose chemotherapy. The inclusion occurs at our center during preparation for blood stem cell transplantation. The written consent will be obtained separately in the context of the information on blood stem cell transplantation. Participation is voluntary and consent can be revoked at any time. This involves no additional effort for the patient and has no influence on his treatment. It may be necessary in the course of contacting the patient at home, as long as the data is incomplete. This is also explicitly explained. A copy of the declaration of consent is given to the patient. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04263857
Study type Observational [Patient Registry]
Source Technical University of Munich
Contact Mareike Verbeek, MD
Phone +49 89 4140
Email mareike.verbeek@tum.de
Status Recruiting
Phase
Start date November 1, 2017
Completion date November 2037

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