Ignite Creation Date:
2024-06-16 @ 11:52 AM
Last Modification Date:
2024-10-26 @ 3:31 PM
Study NCT ID:
NCT06450353
Status:
RECRUITING
Last Update Posted:
2024-06-10
First Post:
2024-05-31
Brief Title:
Prospective Evaluation of Disparities in Provision of Allogeneic Transplantation
Sponsor:
MD Anderson Cancer Center
Organization:
MD Anderson Cancer Center
Study Overview
Official Title:
Prospective Evaluation of Disparities in Provision of Allogeneic Transplantation
Status:
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:
To look at the effect of a recipients ancestry and socio-economic status on their choice of bone marrow transplantation donor cells and their chance of receiving genetically similar allogeneic bone marrow cells versus cells that are not genetically similar allograft
Detailed Description:
Primary Objectives To prospectively evaluate graft options and choice of donor by patient ancestry and SES for allograft candidates at MDACC
Secondary Objectives
To prospectively evaluate time to transplant for allograft candidates at MDACC
To evaluate treatment-related mortality for allograft candidates at MDACC
To assess overall survival for allograft candidates at MDACC
To prospectively evaluate receipt of preferred unrelated donor for allograft recipients at MDACC
To evaluate receipt of an optimal graft for allograft recipients at MDACC
Secondary Objectives
To prospectively evaluate time to transplant for allograft candidates at MDACC
To evaluate treatment-related mortality for allograft candidates at MDACC
To assess overall survival for allograft candidates at MDACC
To prospectively evaluate receipt of preferred unrelated donor for allograft recipients at MDACC
To evaluate receipt of an optimal graft for allograft recipients at MDACC
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
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| NCI-2024-04790 | OTHER | NCI-CTRP Clinical Registry | None |