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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00186290
Other study ID # BMT34
Secondary ID 74165BMT34
Status Completed
Phase N/A
First received September 13, 2005
Last updated October 7, 2010
Start date December 1989
Est. completion date October 2009

Study information

Verified date October 2010
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

To evaluate the role of ablative allogeneic hematopoietic cell transplantation in the treatment of advanced leukemia or lymphoma.


Description:

To determine the disease free survival and overall survival of patients with ALL and ANLL after induction failure, in relapse, or subsequent remission from CML in several phases or recurrent lymphoblastic lymphoma who receive fractionated TBI, etoposide and cyclophosphamide followed by allogenic bone marrow grafting from histocompatible sibling donors. Fractionated Total Body Irradiation (FTBI), Etoposide (VP-16) and Cyclophosphamide (CY) Followed by Allogeneic Bone Marrow Transplantation for Patients with Advanced Leukemia or High Grade Lymphoma


Recruitment information / eligibility

Status Completed
Enrollment 145
Est. completion date October 2009
Est. primary completion date October 2009
Accepts healthy volunteers No
Gender Both
Age group N/A to 50 Years
Eligibility Inclusion Criteria:HLA identical donor

- adequate organ function

- other life threatening disease

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


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 overall survival october 2009 No
Primary disease free survival October 2009 No
Secondary early and late toxicities of the treatment regimen October 2009 Yes
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