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Registry Study of T Cell Depleted Allo Non-Myeloablative Stem Cell Transplant

Registry Study of T Cell Depleted Allogeneic Non-Myeloablative Stem Cell Transplant Recipients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01904175
Enrollment
48
Registered
2013-07-22
Start date
2013-08-31
Completion date
2016-04-30
Last updated
2016-05-05

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

Conditions

Hodgkin's Disease, Leukemia, Myelodysplasia, Myeloma, Non Hodgkin's Lymphoma

Keywords

Stem cell transplantation, non-myeloablative

Brief summary

Allogeneic transplantation is used to treat many malignant and non-malignant diseases. The investigators and others have shown that less toxic preparative regimens (reduced intensity or 'mini' transplants) allow reliable allogeneic engraftment and durable remissions, significantly broadening the population of patients who may be offered this therapy to those who are older and more infirmed. The field is now focusing on the period post transplant for approaches to immune recovery leading to improved outcomes. The primary objective of this registry is to catalogue data from patients who undergo standard of care reduced intensity allogeneic transplantation.

Detailed description

Subjects will have toxicity monitored and reported per the Center for International Blood and Marrow Transplant Research (CIBMTR) program standard and as required by law for bone marrow transplant (BMT) reporting in the USA. Data will be collected from physical exam, laboratory studies, radiographs that are performed for clinical purposes. The tests and procedures are not in addition or in excess of our standards for allogeneic transplant outside of this registry. Data about donors will also be collected.

Interventions

None listed

Sponsors

Duke University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

Recipient Inclusion Criteria: * Subjects ≥ 18 years of age undergoing a reduced intensity allogeneic transplant

Exclusion criteria

* Subjects \< 18 years of age * Subjects not undergoing nonmyeloablative or ablative allogeneic transplant

Design outcomes

Primary

MeasureTime frameDescription
Catalogue Data1 yearCatalogue data from subjects who undergo standard of care reduced intensity allogeneic transplantation.

Countries

United States

Outcome results

None listed

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