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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00186225
Other study ID # IRB-13390
Secondary ID 75268BMT22
Status Completed
Phase N/A
First received
Last updated
Start date November 1989
Est. completion date May 2010

Study information

Verified date April 2020
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the use of unrelated donors for hematopoietic cell transplantation in the treatment of hematologic and lymphoid malignancies.


Description:

Stem Cell Transplantation from Matched Unrelated or Partially Matched Related Donors Using a Preparatory Regimen Consisting of Fractionated Total Body Irradiation (FTBI) and Cyclophosphamide (CY). To administer high dose radio-chemotherapy followed by stem cell transplantation from a matched unrelated donor or a partially matched related donor.


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date May 2010
Est. primary completion date June 2007
Accepts healthy volunteers No
Gender All
Age group N/A to 50 Years
Eligibility Inclusion Criteria:- acute leukemia

- chronic leukemia

- lymphoblastic lymphoma

- MDS

- MPS Exclusion Criteria:- organ dysfunction

- HIV positive

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ablative allogeneic hematopoietic cell transplantation


Locations

Country Name City State
United States Stanford University School of Medicine Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary oxicity and efficacy of TBI and cyclophosphamide as preparation for hematopoietic cell transplantation from partially matched and unrelated donors.
Secondary Overall Survival
Secondary Event Free Survival
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