Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
5000 participants
OBSERVATIONAL
2017-11-01
2037-11-30
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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OTHER
OTHER
Eligibility Criteria
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Inclusion Criteria
* patients eligible for stem cell transplantation
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Technical University of Munich
OTHER
Responsible Party
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Principal Investigators
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Mareike Verbeek, MD
Role: PRINCIPAL_INVESTIGATOR
Klinikum rechts der Isar der TU Munich, Germany
Locations
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Klinikum rechts der Isar der TU München
Munich, , Germany
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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REBB3M
Identifier Type: -
Identifier Source: org_study_id