1200 Participants Needed

Patient Ancestry Questionnaires for Transplant

WF
Overseen ByWarren Fingrut, MD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: M.D. Anderson Cancer Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores how a person's background and economic status might affect their choice and success with bone marrow transplants. It examines whether individuals receive genetically similar (closer match) bone marrow. Participants will complete a questionnaire about their family background, and researchers will use medical records to track health outcomes. Eligible participants are those planning to undergo a bone marrow transplant. As an unphased trial, participation offers a unique opportunity to contribute to understanding how personal factors influence transplant success.

Do I need to stop my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications.

Why are researchers excited about this trial?

Researchers are excited about this trial because it aims to uncover disparities in the provision of allogeneic bone marrow transplantation, a key treatment for various blood cancers and disorders. Unlike most studies that focus on the medical aspects alone, this trial digs into social and demographic factors to see how they influence access to this life-saving treatment. By collecting detailed information on participants' demographics and health outcomes, researchers hope to identify and address barriers, ensuring more equitable access to transplantation for all patients. This could lead to significant improvements in healthcare fairness and outcomes.

Who Is on the Research Team?

WF

Warren Fingrut, MD

Principal Investigator

M.D. Anderson Cancer Center

Are You a Good Fit for This Trial?

Inclusion Criteria

I am eligible for a transplant from a donor.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Consent and Questionnaire

Participants sign the consent form and complete a questionnaire about their demographic information and ancestry

1 day
1 visit (in-person)

Data Collection

Information about the participants' medical history, choice of bone marrow donor, and health outcomes is collected from medical records

Up to 2 years

Follow-up

Participants are monitored for safety and effectiveness after transplantation

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Patient Ancestry Questionnaires

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Prospective evaluationExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

M.D. Anderson Cancer Center

Lead Sponsor

Trials
3,107
Recruited
1,813,000+