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Risk Factors for Cytomegalovirus Disease in Solid Organ Transplantation

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00170170
Recruitment Status : Completed
First Posted : September 15, 2005
Last Update Posted : February 2, 2010
Sponsor:
Collaborator:
Information provided by:

Study Description
Brief 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.

Condition or disease
Transplantation Infection Cytomegalovirus Infections

Detailed 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.

Study Design

Study Type : Observational
Actual Enrollment : 500 participants
Time Perspective: Retrospective
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
Study Start Date : November 2004
Primary Completion Date : June 2007
Study Completion Date : June 2007

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Groups and Cohorts


Outcome Measures

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Recipients of liver, kidney, pancreas, heart or lung transplantation
Criteria

Inclusion Criteria:

  • Recipients of liver, kidney, pancreas, heart or lung transplantation
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00170170


Locations
United States, Minnesota
Mayo Clinic
Rochester, Minnesota, United States, 55905
Sponsors and Collaborators
Mayo Clinic
Roche Pharma AG
Investigators
Principal Investigator: Raymund R. Razonable, M.D. Mayo Clinic
More Information

ClinicalTrials.gov Identifier: NCT00170170     History of Changes
Other Study ID Numbers: 2275-04
VAL101
First Posted: September 15, 2005    Key Record Dates
Last Update Posted: February 2, 2010
Last Verified: February 2010

Keywords provided by Mayo Clinic:
cytomegalovirus

Additional relevant MeSH terms:
Infection
Communicable Diseases
Cytomegalovirus Infections
Herpesviridae Infections
DNA Virus Infections
Virus Diseases