Register of patients undergoing blood stem cell transplantation
Official title: Register of Survey and Evaluation of Blood Stem Cell Transplantations of Clinic III of Internal Medicine III
Run by Technical University of Munich · NCT04263857 · Data updated 2026-11-12
This study is tracking patients who have had blood stem cell transplants for blood cancers to see how well they do and what complications they might face.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 5000 (estimated) |
| Sponsor | Technical University of Munich Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Munich) |
| Status | Recruiting |
| Started | November 1, 2017 |
| Main results expected | November 2037 |
| Study ends | November 2037 |
| Registry record updated | November 24, 2023 |
| Trial ID | NCT04263857 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients who are eligible for blood stem cell transplantation and have provided informed consent.
✕Probably not a fit
Patients who are unable to consent to study participation will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study documents patients who have received autologous or allogenic blood stem cell transplants for hematologic malignancies. It focuses on collecting data regarding complication rates, disease response, survival rates, engraftment, and transplantation settings, including donor and conditioning information. Patients are included during their preparation for transplantation, and their participation is voluntary with the option to withdraw at any time. The study aims to enhance understanding of transplantation outcomes without imposing additional burdens on participants.
Why it matters
Potential benefit: If successful, this study could improve patient outcomes by providing valuable insights into the effectiveness and safety of blood stem cell transplantation.
How similar studies have gone: Other studies have documented outcomes of blood stem cell transplantation, indicating that this approach builds on existing knowledge rather than being entirely novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * signed IC * patients eligible for stem cell transplantation Exclusion Criteria: * unable to consent to study participation
Where it's running
-
Klinikum rechts der Isar der TU München
Munich, Germany Recruiting
Study contacts
- Principal investigator: Mareike Verbeek, MD — Klinikum rechts der Isar der TU Munich, Germany
- Study coordinator: Mareike Verbeek, MD
- Email: mareike.verbeek@tum.de
- Phone: +49 89 4140
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Tempus Open Link registry for cancer patients using Olivia platform
This registry tests whether Olivia can securely enroll cancer patients and combine their health data from EHRs and patient-reported outcomes to build a large, de-identified dataset.
-
Genetics of Blood Cancers in the U.S. population
This study tests how genetic factors relate to blood cancers by collecting saliva DNA and online health surveys from at least 10,000 U.S. adults.
-
Leflunomide to prevent CMV reactivation after haploidentical stem cell transplant
This study tests whether leflunomide can prevent CMV reactivation in adults undergoing haploidentical hematopoietic stem cell transplantation.
-
MK-1045-006: testing a new treatment for B-cell cancers like CLL and SLL
This trial will test MK-1045 in people with relapsed or treatment‑refractory CLL/SLL to see if it’s safe and how well it works.
-
Predicting bleeding risk in patients with severe thrombocytopenia using a viscoelastic and clinical score
We test a new score that combines viscoelastic test results with clinical data to see if we can predict bleeding risk in adults with malignant hematologic disorders and very low platelets.
-
Ruxolitinib to prevent graft-versus-host disease after allogeneic stem cell transplant
This trial will test whether adding ruxolitinib to standard drugs better prevents chronic graft-versus-host disease in adults receiving an allogeneic stem cell transplant for blood cancers.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.