Viewing Study NCT06452732



Ignite Creation Date: 2024-06-16 @ 11:52 AM
Last Modification Date: 2024-10-26 @ 3:31 PM
Study NCT ID: NCT06452732
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-14
First Post: 2024-06-05

Brief Title: Using Multiparametric Flow Cytometry to Detect Peripheral Blood and Bone Marrow Leukaemia Stem Cells for Relapse Prediction in P-AML
Sponsor: Peking University Peoples Hospital
Organization: Peking University Peoples Hospital

Study Overview

Official Title: Using Multiparametric Flow Cytometry to Detect Peripheral Blood and Bone Marrow Leukaemia Stem Cells for Relapse Prediction in Pediatric Acute Myeloid Leukaemia a Prospective Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
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: None
Brief Summary: Leukaemia is a major disease that seriously endangers human health the long-term survival rate of acute myeloid leukaemia receiving conventional chemotherapy is only 10 to 45 haematological relapse is the main cause of treatment failure in acute myeloid leukaemia reducing the relapse rate is the key to improving the efficacy of acute leukaemia biomarker-guided preemptive therapy is an effective way to reduce the recurrence of leukaemia existing markers to predict the recurrence has a high false Existing markers have high false-negative and false-positive rates for predicting relapse and improving the accuracy of leukaemia relapse prediction is a major clinical problem that needs to be solved urgently The group has found that circulating leukaemia stem cells remaining after chemotherapy are the key to relapse therefore we propose to conduct a multicentre prospective clinical study on the prediction of acute leukaemia relapse by circulating leukaemia stem cells
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