Register of Blood Stem Cell Transplantation

  • STATUS
    Recruiting
  • End date
    Nov 28, 2037
  • participants needed
    5000
  • sponsor
    Technische Universität München
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Updated on 16 February 2024
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cell transplantation

Summary

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

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.

Details
Condition Hematologic Malignancy, Blood disorder
Age 18years - 100years
Clinical Study IdentifierNCT04263857
SponsorTechnische Universität München
Last Modified on16 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

signed IC
patients eligible for stem cell transplantation

Exclusion Criteria

unable to consent to study participation
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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