Viewing Study NCT06362720



Ignite Creation Date: 2024-05-06 @ 8:24 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06362720
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-04-12
First Post: 2024-04-03

Brief Title: The Comparison the CMV Infection and Reactivation After Allogeneic Hematopoietic Stem Cell Transplantation Between Standard Regimen Methotrexate Plus Cyclosporin A and Post-transplant Cyclophosphamide-based Regimen
Sponsor: Siriraj Hospital
Organization: Siriraj Hospital

Study Overview

Official Title: The Comparison the CMV Infection and Reactivation After Allogeneic Hematopoietic Stem Cell Transplantation Between Standard Regimen Methotrexate Plus Cyclosporin A and Post-transplant Cyclophosphamide-based Regimen
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CMV
Brief Summary: The goal of this observational study is to compare the CMV infection and reactivation after allogeneic hematopoietic stem cell transplantation Between Standard Regimen Methotrexate plus Cyclosporin A and Post-transplant Cyclophosphamide-based Regimen The main questions it aims to answer are

How do CMV infection and reactivation differ between Allo-SCT patients who received a standard regimen versus those who received a Post-transplant Cyclophosphamide-based regimen
progression-free survival Median overall survival cumulative incidence of relapse non-relapsed mortality NRM and GvHD at 2 years after Allo-SCT
The impact of CMV infection and CMV reactivation on progression-free survival overall survival and NRM
Averse events of GVHD prophylaxis medication Participants will be collected the data of treatment and treatment response during transplant until 2 years after transplant from hospital medical record
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None