Viewing Study NCT01596257



Ignite Creation Date: 2024-05-06 @ 12:30 AM
Last Modification Date: 2024-10-26 @ 10:51 AM
Study NCT ID: NCT01596257
Status: COMPLETED
Last Update Posted: 2022-12-29
First Post: 2012-05-09

Brief Title: Bulk Versus Fractionated Stem Cell Infusions in Patients With Hematologic Malignancies Undergoing Stem Cell Transplantation
Sponsor: Memorial Sloan Kettering Cancer Center
Organization: Memorial Sloan Kettering Cancer Center

Study Overview

Official Title: Randomized Phase II Trial of Bulk Versus Fractionated Stem Cell Infusions in Patients With Hematologic Malignancies Undergoing Stem Cell Transplantation
Status: COMPLETED
Status Verified Date: 2021-08
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 purpose of this study is to find out if getting a blood stem cell transplant with donor stem cells given over several days is better than getting a blood stem cell transplant with donor stem cells given over 1 day We want to find out which procedure over will result in improved recovery of blood and immune function after transplant When donor stem cells are given over various days in mice the blood and immune system recovery is quicker
Detailed Description: This is a complex study that involves various interventions Intervention 1 Donor Initial Stem Cell Collection Intervention 2 Stem Cell Product Initial Processing Orders Intervention 3 Patient Admission and Transplantation Intervention 4 Stem cell infusion Intervention 5 Post infusion follow up Intervention 6 Off Study Patient and Donor Evaluation

Patients whose donor fails to collect the appropriate number of cells will receive all their cells as a bulk infusion These patients will continue to receive a transplant on protocol but will be replaced until both arms have reached the target accrual

Study Oversight

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