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ACB A Randomized Study of 2.5ug/kg/Day vs. 5ug/kg/Day Dose of G-CSF After High Dose Chemotherapy Followed by Autologous Peripheral Blood Stem Cell/Marrow Transplant Recipients FILE#17159
This study has been completed.
Sponsored by: Alberta Cancer Board
Information provided by: Alberta Cancer Board
ClinicalTrials.gov Identifier: NCT00168168
  Purpose

Evaluate recovery time on 2.5 mg/Kg/day dose of G-CSF versus 5 mg/Kg/day dose.


Condition Intervention
Peripheral Stem Cell/Marrow Transplant
Drug: G-CSF/Filgrastim

Drug Information available for: Filgrastim Granulocyte colony-stimulating factor
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Dose Comparison, Single Group Assignment, Safety/Efficacy Study
Official Title: ACB A Randomized Study of 2.5ug/kg/Day vs. 5ug/kg/Day Dose of G-CSF After High Dose Chemotherapy Followed by Autologous Peripheral Blood Stem Cell/Marrow Transplant Recipients FILE#17159

Further study details as provided by Alberta Cancer Board:

Estimated Enrollment: 60
Study Start Date: July 2003
Study Completion Date: February 2007
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • over age 18
  • autologous stem cell/marrow transplant candidate in MM, lymphoma, AMG and testicular

Exclusion Criteria:

  • age below 18 years
  • sensitive to G-CSF
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00168168

Locations
Canada, Alberta
Cross Cancer Institute
Edmonton, Alberta, Canada
Sponsors and Collaborators
Alberta Cancer Board
Investigators
Principal Investigator: Meluka Game, MD Alberta Cancer Board
  More Information

Study ID Numbers: HE-10-0053
Study First Received: September 14, 2005
Last Updated: September 22, 2008
ClinicalTrials.gov Identifier: NCT00168168  
Health Authority: Canada: Health Canada

Keywords provided by Alberta Cancer Board:
G-CSF
Filgrastim
Engraftment time
Autologus transplant

ClinicalTrials.gov processed this record on January 13, 2009