Register of Survey and Evaluation of Blood Stem Cell Transplantations of Clinic III of Internal Medicine III
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 5,000
- Locations
- 1
- Primary Endpoint
- Register of stem cell transplantation
Study Overview
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.
Study Design
- Study Type
- Observational
- Observational Model
- Other
- Time Perspective
- Other
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •signed IC
- •patients eligible for stem cell transplantation
Exclusion Criteria
- •unable to consent to study participation
Outcomes
Primary Outcomes
Register of stem cell transplantation
Time Frame: approximately over 20 years
Recording of all stem cell transplantations over many years
Secondary Outcomes
- Register of survivals(approximately over 20 years)
- Register of toxicities(approximately over 20 years)
- Register of complications(approximately over 20 years)
- Register of morbidities(approximately over 20 years)
