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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00170170
Other study ID # 2275-04
Secondary ID VAL101
Status Completed
Phase N/A
First received September 13, 2005
Last updated February 1, 2010
Start date November 2004
Est. completion date June 2007

Study information

Verified date February 2010
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This study will investigate the clinical variables that may be used to predict who among the solid organ transplant recipients will develop cytomegalovirus (CMV) disease after completing antiviral prophylaxis.


Description:

This study will investigate the clinical and laboratory variables that may be used to predict who among the solid organ transplant recipients will develop CMV disease after completing antiviral prophylaxis. This is a retrospective study of patients seen at the Mayo Clinic during the past five years.


Recruitment information / eligibility

Status Completed
Enrollment 500
Est. completion date June 2007
Est. primary completion date June 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Recipients of liver, kidney, pancreas, heart or lung transplantation

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Mayo Clinic Rochester Minnesota

Sponsors (2)

Lead Sponsor Collaborator
Mayo Clinic Roche Pharma AG

Country where clinical trial is conducted

United States, 

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