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NCT00569842 Clinical Trial

Investigation of the Cylex® ImmuKnow® Assay

Multiple Myeloma Clinical Trial

Official title:
Investigation of the Cylex® ImmuKnow® Assay

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00569842
Other study ID # 0710-11/ IUCRO-0207
Secondary ID
Status Completed
Phase N/A
First received December 5, 2007
Last updated September 10, 2014
Start date November 2007
Est. completion date December 2012

Study information
Verified date September 2014
Source Indiana University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Currently, there is no accurate way of predicting the occurrence of Graft vs Host Disease (GvHD) or infection. The purpose of this study is to analyze blood with the ImmuKnow® Assay to see if doctors can detect which patients are at risk for GvHD and for getting an infection before they occur.

Recruitment information / eligibility
Status Completed
Enrollment 45
Est. completion date December 2012
Est. primary completion date February 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

Patients who are undergoing allogeneic HSCT using a myeloablative preparative regimen for any of the following disorders are eligible:

1. Acute leukemia

2. Non-Hodgkin's Lymphoma

3. Chronic lymphocytic leukemia

4. Hodgkin's disease

5. Multiple myeloma

6. Myelodysplastic Syndromes

7. Myeloproliferative Disorders

8. Aplastic Anemia

9. Chronic myelogenous leukemia

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Indiana Universtiy Simon Cancer Center Indianapolis Indiana

Sponsors (1)
Lead Sponsor Collaborator
Indiana University School of Medicine

Country where clinical trial is conducted

United States, 

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