Viewing Study NCT06302699



Ignite Creation Date: 2024-05-06 @ 8:14 PM
Last Modification Date: 2024-10-26 @ 3:23 PM
Study NCT ID: NCT06302699
Status: RECRUITING
Last Update Posted: 2024-03-12
First Post: 2024-03-04

Brief Title: Detecting Minimal Residual Diseases MRD and Monitoring Clonal Evolution Using Ultrasensitive Chromosomal Aberrations Detection UCAD in Multiple Myeloma
Sponsor: Institute of Hematology Blood Diseases Hospital China
Organization: Institute of Hematology Blood Diseases Hospital China

Study Overview

Official Title: Clinical Utility of Ultrasensitive Chromosomal Aberrations Detection UCAD for Detecting Minimal Residual Disease MRD and Monitoring Clonal Evolution by Low-Pass Whole Genome Sequencing in Multiple Myeloma
Status: RECRUITING
Status Verified Date: 2024-03
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: The presence of minimal residual disease MRD is an important prognostic factor for multiple myeloma while copy number variation CNV is a widely accepted biomarker used for multiple myeloma MM Detecting MRD and monitoring clonal evolution by monitoring CNV using low-pass whole genome sequencing is promising due to its high analytical sensitivity To evaluate the correlation between MRD detected by flow cytometry and low-pass whole genome sequencing nearly 200 samples were collected for this study We applied ultrasensitive chromosomal aberrations detection to detect CNV for each patient The follow-up samples were then collected and sequencing used the same method
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?: False
Is an FDA AA801 Violation?: None