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Register of Blood Stem Cell Transplantation

Register of Survey and Evaluation of Blood Stem Cell Transplantations of Clinic III of Internal Medicine III

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04263857
Acronym
REBB3M
Enrollment
5000
Registered
2020-02-11
Start date
2017-11-01
Completion date
2037-11-30
Last updated
2023-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hematologic Malignancies

Keywords

autologous & allogenic blood stem cell transplantations

Brief summary

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

Detailed 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.

Interventions

None listed

Sponsors

Technical University of Munich
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* signed IC * patients eligible for stem cell transplantation

Exclusion criteria

* unable to consent to study participation

Design outcomes

Primary

MeasureTime frameDescription
Register of stem cell transplantationapproximately over 20 yearsRecording of all stem cell transplantations over many years

Secondary

MeasureTime frameDescription
Register of toxicitiesapproximately over 20 yearsRecording of toxicities occured during and after SCT according to GvHD Score Standards and blood and bone marrow samples, and Imaging (CT Scans)
Register of complicationsapproximately over 20 yearsRecording of complications occurred during and after SCT in Terms of infectious complications and occurance of GvHD (according to GvHD Score and Imaging and clinical assessment)
Register of morbiditiesapproximately over 20 years
Register of survivalsapproximately over 20 yearsRecording of survival Status, Assessment of Remission Status by bone marrow and blood diagnostics, clinical follow up

Countries

Germany

Contacts

Primary ContactMareike Verbeek, MD
mareike.verbeek@tum.de+49 89 4140

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026