Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06916195

Burden of Cytomegalovirus Reactivation in Pediatric Patients After Allogeneic Hematopoietic Stem Cell Transplantation

CMV PED Study - A Retrospective Observational Study To Understand The Clinical And Economic Burden Associated With Cytomegalovirus Reactivation and Related Health Outcomes In Pediatric Patients Receiving Allogeneic Hematopoietic Stem Cell Transplantation In Italy

Status
Recruiting
Phase
Study type
Observational
Enrollment
230 (estimated)
Sponsor
MSD Italia S.r.l. · Industry
Sex
All
Age
0 Years – 18 Years
Healthy volunteers
Not accepted

Summary

This observational retrospective analysis will provide useful information for clinicians and payers, and local guidelines committee members, to improve the understanding of Cytomegalovirus clinical and economic burden and clinical management of pediatric patients undergoing allogeneic Hematopoietic Stem Cells Transplantation in Italy.

Detailed description

This is an observational retrospective analysis from the main pediatric centers in Italy (approximately 5 sites). The selected sites will be the most representative of Italy because they perform about 2/3 of all allogeneic HSCT per year. Index date: date of allogeneic HSCT; retrospective data will be captured in consecutive patients undergoing allogeneic HSCT from January 2018 to June 2020 with maximum 12 months of follow-up for each patient. The data of the patients undergoing allogeneic HSCT after June 2020 will not be captured in order to avoid any possible bias due to off-label access to letermovir. Medical Records (MR) will be used to describe the risk factors, patient characteristics, treatment patterns, and healthcare resource utilization of subjects who had a CMV infection. Electronic or paper hospital charts (inpatient), clinical charts (inpatient and outpatient), and outpatient records will all be considered as MR for study purposes. This is a secondary data collection study from electronic or paper medical chart review, no data from registry will be collected. Patients (or their legally acceptable representatives) must have signed and dated the Informed Consent \& Privacy Form (ICF), if applicable.

Conditions

Timeline

Start date
2025-05-09
Primary completion
2026-04-30
Completion
2026-07-15
First posted
2025-04-08
Last updated
2026-04-06

Locations

5 sites across 1 country: Italy

Source: ClinicalTrials.gov record NCT06916195. Inclusion in this directory is not an endorsement.