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NCT00170170 Clinical Trial

Risk Factors for Cytomegalovirus Disease in Solid Organ Transplantation

Infection Clinical Trial

Official title:
Clinical Predictors of Late-onset CMV Disease in Solid Organ Transplant Recipients: A Strategy to Improve the Benefits and Reduce the Risks of Anti-CMV Prophylaxis

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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