Skip to content

Dendritic Cells in Patients Following Allogeneic Hematopoietic Stem Cell Transplantation

Analysis of Dendritic Cells in Patients Following Allogeneic Hematopoietic Stem Cell Transplantation

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00450268
Acronym
DCalloTX
Enrollment
50
Registered
2007-03-22
Start date
2005-01-31
Completion date
2010-01-31
Last updated
2007-03-22

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

Conditions

Graft Versus Host Disease

Keywords

Graft versus host disease, Allogeneic hematpoietic stem cell transplantation

Brief summary

We plan to investigate prospectively and simultaneously skin and blood DC subtypes, their donor/recipient origin and the correlation of DC reconstitution kinetics with treatment, clinical outcome and incidence of aGvHD in patients undergoing allogeneic hematopoietic stem cell transplantation.

Detailed description

Blood and skin DC reconstitution shall be investigated in patients affected by hematological diseases and receiving HLA-matched, mobilized peripheral blood stem cells from related or unrelated donors. We plan to simultaneously collect and process double biopsies, i.e. from graft versus host disease affected and non-lesional skin of patients at onset of acute graft versus host disease following allogeneic hematopoietic stem cell transplantation. Emigration assay, Chimerism analysis and immunohistochemistry will be performed.

Interventions

PROCEDUREblood draw, skin shave biopsy

Sponsors

Technische Universität Dresden
Lead SponsorOTHER

Study design

Observational model
DEFINED_POPULATION
Time perspective
OTHER

Eligibility

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

Inclusion criteria

* Patient undergoing an allogeneic hematopoietic stem cell transplantation * Older than 18 years * WHO-Performance-Status 0 to3 * Informed consent * Graft versus host disease of the skin

Exclusion criteria

* Clotting parameters more than double of normal * Infection of the skin * Leucocytes \< 1000/µl; Thrombocytes \< 20 000/µl

Countries

Germany

Contacts

Primary ContactSusanne Gretzinger, MD
susanne.gretzinger@uniklinik-dresden.de+49 351 458
Backup ContactMartin Bornhäuser, Professor
martin.bormhaeuser@uniklinik-dresden.de*49 351 458

Outcome results

None listed

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