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Cytomegalovirus Resistance in Transplant Patients and Bone Marrow Recipients in the Prophylaxis Era, a French Multicentric Cohort Study
The investigators aim is to determine the incidence of cytomegalovirus resistance to antivirals in a cohort study. The patients are included at their first CMV active infection and are followed during two years thereafter. When criteria for suspected resistance are meet, blood and urine samples are collected for virus isolation and further resistance phenotype, and for resistance genotype determination. Results are compared with baseline samples. Clinical information such as treatment, immunosuppressive regimen and clinical evolution will be collected. Through this study, the investigators aim to organize a national network for the detection and identification of CMV resistant strains that will be useful when new therapeutics will be available.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Virologie
Amiens, France
Virologie
Angers, France
Virologie
Besançon, France
Virologie - Hôpital Avicenne
Bobigny, France
Virologie
Bordeaux, France
Virologie
Brest, France
Virologie
Caen, France
Virologie
Clermont-Ferrand, France
Virologie
Dijon, France
Virologie
Fort de France, France
Start Date
August 1, 2006
Primary Completion Date
December 1, 2010
Completion Date
June 1, 2012
Last Updated
July 20, 2025
800
ESTIMATED participants
depistage
BIOLOGICAL
Lead Sponsor
University Hospital, Limoges
NCT06439342
NCT05664126
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT06958796