Clinical Trials Directory

Trials / Completed

CompletedNCT01779882

Cyclophosphamide and Busulfan as Conditioning Regimen Before Allogeneic HSCT

Cyclophosphamide-Busulfan Versus Busulfan-Cyclophosphamide as Conditioning Regimen Before Allogeneic Hematopoietic Stem Cell Transplantation for Leukemia: a Prospective Randomized Study to Assess Liver Toxicity

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
72 (actual)
Sponsor
University Hospital, Basel, Switzerland · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to test the hypothesis, that the order of application of Busulfan (BU) and Cyclophosphamide (CY) has an impact on toxicity after allogeneic Hematopoietic stem cell transplantation (HSCT) and that CY-BU reduces liver toxicity compared to BU-CY.

Conditions

Interventions

TypeNameDescription
DRUGBusulfan-Cyclophosphamide as Conditioning Regimen before Allogeneic Hematopoietic Stem Cell TransplantationTest the hypothesis, that the order of application of Busulfan (BU) and Cyclophosphamide (CY) has an impact on toxicity after allogeneic Hematopoietic stem cell transplantation (HSCT) and that CY-BU reduces liver toxicity compared to BU-CY.
DRUGCyclophosphamide-Busulfan as Conditioning Regimen before Allogeneic Hematopoietic Stem Cell TransplantationTest the hypothesis, that the order of application of Busulfan (BU) and Cyclophosphamide (CY) has an impact on toxicity after allogeneic Hematopoietic stem cell transplantation (HSCT) and that CY-BU reduces liver toxicity compared to BU-CY.

Timeline

Start date
2013-01-01
Primary completion
2018-01-06
Completion
2018-01-06
First posted
2013-01-30
Last updated
2018-03-02

Locations

3 sites across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT01779882. Inclusion in this directory is not an endorsement.