Clinical Trials Logo

Clinical Trial Summary

Disseminated Adv infections are associated with high morbidity and mortality in HSCT pediatric patients. The most common source of Adv infection after pediatric HSCT is the host digestive tract where latent Adv are reactivated after engraftment. We have shown in a monocentric study that Adv viral load in stools is a predictive factor of blood infection in children with digestive Adv infections. We assume that an early treatment, with antiviral drugs, such as cidofovir and brincidofovir, may avoid severe Adv infections and diseases and thus that molecular surveillance in stool is a critical factor for the control of Adv reactivations.

The study has two main objectives: (i) confirming the impact of Adv viral load in stools on the occurrence of blood infection based on a multicentric prospective cohort study design; and (ii) determining the prognostic and predictive factors for efficacy and toxicity of antiviral drugs, such as brincidofovir and cidofovir.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03481244
Study type Observational
Source Assistance Publique - Hôpitaux de Paris
Contact Jérôme Le GOFF, MDPhD
Phone 33+1 42499493
Email jerome.le-goff@aphp.fr
Status Not yet recruiting
Phase
Start date April 2020
Completion date December 2023