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Incidence and Outcomes Associated With the Management of Adenovirus Infections in Allogenic Hematopoietic Cell Transplant Recipients

Incidence and Outcomes Associated With the Management of Adenovirus Infections in Allogeneic Hematopoietic Cell Transplant Recipients: AdVance

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04285788
Acronym
AdVance
Enrollment
216
Registered
2020-02-26
Start date
2013-01-31
Completion date
2017-01-31
Last updated
2022-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adenovirus Infections, Human

Brief summary

To depict the incidence, outcomes and standards of care (SoC) of adenovirus (AdV) infections and associated practice patterns in allogeneic hematopoietic cell transplant recipients. It is expected that participating centers will be in the United Kingdom, France, Spain, Germany, and Italy.

Interventions

None listed

Sponsors

Jazz Pharmaceuticals
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Months to 90 Years
Healthy volunteers
No

Inclusion criteria

* At least one AdV positive test, regardless of specimen within 6 months following the first allo-HCT * Subjects first allo-HCT must have been performed between 1 January 2013 and 30 September 2015

Exclusion criteria

* AdV negative

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with non-relapse related mortality 3 and 6 months after first AdV Virema in paediatric allo-HCT recipients3 and 6 months after first adenovirus viremiaTo assess non-relapse related mortality 3 to 6 months after first adenovirus viremia.

Secondary

MeasureTime frameDescription
Number of participants who were hospitalized To assess the number of hospitalizations3 to 6 monthsTo assess the number of hospitalizations, length of stay, and ICU stay.
The rate of adenovirus infection progression3 to 6 monthsTo assess the rate of progression to disseminated adenovirus disease within the first year following allo-HCT

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026