Enrichment & Purging of Stem Cells in Non-Hodgkin's Lymphoma

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Stanford University
ClinicalTrials.gov Identifier:
NCT00186355
First received: September 13, 2005
Last updated: May 10, 2012
Last verified: May 2012

September 13, 2005
May 10, 2012
October 2003
March 2007   (final data collection date for primary outcome measure)
PCR positivity in peripheral blood cell collections after cyclophosphamide [ Time Frame: unknown ] [ Designated as safety issue: No ]
PCR positivity in peripheral blood cell collections after cyclophosphamide
Complete list of historical versions of study NCT00186355 on ClinicalTrials.gov Archive Site
Enrichment of hematopoietic stem cells [ Time Frame: unknown ] [ Designated as safety issue: No ]
  • - Enrichment of hematopoietic stem cells
  • - Engraftment
Not Provided
Not Provided
 
Enrichment & Purging of Stem Cells in Non-Hodgkin's Lymphoma
Enrichment and Purging of Stem Cells in the Treatment of Non-Hodgkin's Lymphoma

To evaluate the role of purging the hematopoietic cell graft on outcomes for non-Hodgkin's Lymphoma.

To study the use of peripheral blood stem cells which have been treated in an effort to remove tumor cells. The researchers hope to learn whether or not this will be more effective in removing the tumor cells as compared to other methods of purging (the removal of cancer cells).

Interventional
Not Provided
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Lymphoma, Non-Hodgkin
Procedure: high dose chemo then auto hematopoietic cell transplant
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
97
February 2010
March 2007   (final data collection date for primary outcome measure)

Inclusion Criteria:- relapsed NHL

Exclusion Criteria:- liver dysfunction

Both
up to 75 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00186355
BMT4IJ, 77063, 12170
Not Provided
Stanford University
Stanford University
National Institutes of Health (NIH)
Principal Investigator: Robert S Negrin Stanford University
Stanford University
May 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP