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Young Adult (18-34)
Transplant
18 studies match your search
By physician referral or invitation only

Pediatric Chronic Kidney Disease Research Registry

We are collecting data on children living with chronic kidney disease, including children on dialysis or with a kidney transplant, to learn more about what happens over time. The data collected will be used for research projects.

Age & Gender
  • 0 years ~ 25 years
  • Male, Female, Gender Inclusive
Study Interest
  • Child and Teen Health
  • Developmental
  • Transplant
  • and 2 more
Visit Location
100% Remote (online, phone, text)
By physician referral or invitation only

10-CBA: A Multicenter Access and Distribution Protocol for Unlicensed Cryopreserved Cord Blood Units (CBUs) for Transplantation in Pediatric and Adult Patients with Hematologic Malignancies and Other Indications

This study is an access and distribution protocol for unlicensed cryopreserved cord blood units (CBUs) in pediatric and adult patients with hematologic malignancies and other indications. This protocol will allow access to cord blood units that are unlicensed.

Age & Gender
  • 1 months ~ 99 years
  • Male, Female, Gender Inclusive
Study Interest
  • Blood Conditions
  • Chronic Conditions
  • Transplant
  • and 2 more
Visit Location
100% Remote (online, phone, text)
By physician referral or invitation only

Comparing Unrelated Donor Bone Marrow Transplant with Immune Suppressive Therapy in Newly Diagnosed Pediatric and Young Adults with Severe Aplastic Anemia

The goal of this study is to determine which treatment option is best to start with for patients with Severe Aplastic Anemia (SAA), between a matched unrelated donor bone marrow transplant or immune suppressive therapy, when a matched related donor is not available.

Age & Gender
  • 1 months ~ 25 years
  • Male, Female, Gender Inclusive
Study Interest
  • Blood Conditions
  • Child and Teen Health
  • Transplant
Visit Location
100% Remote (online, phone, text)
By physician referral or invitation only

Heartcare Outcomes Registry

The purpose of this registry is to observe outcomes of heart transplant recipients who are managed with HeartCare. This is done by collecting information about your heart transplant such as test results, biopsy results, and outcomes, storing that information in a database, and using that information for research.

Age & Gender
  • 21 years ~ 99 years
  • Male, Female
Study Interest
  • Transplant
Visit Location
100% Remote (online, phone, text)
By physician referral or invitation only

Mismatched Unrelated Donor

This study will evaluate the use of MMUD PBSC in adults and explore the safety and efficacy of MMUD BM in pediatric recipients with hematological malignancies who may lack other donor options.

Age & Gender
  • 1 years ~ 66 years
  • Male, Female, Gender Inclusive
Study Interest
  • Cancer (Leukemia)
  • Transplant
Visit Location
100% Remote (online, phone, text)
By physician referral or invitation only

Ventricular Assist Device (VAD) Stressors Study

The purpose of this study is to collect data from patients, caregivers, and VAD coordinators to ascertain the stressors associated with having a Ventricular Assist Device (VAD) and use that data to create support groups.

Age & Gender
  • 18 years ~ 99 years
  • Male, Female, Gender Inclusive
Study Interest
  • Behavior
  • Mental and Emotional Health
  • Transplant
  • and 3 more
Visit Location
100% Remote (online, phone, text)
By physician referral or invitation only

Collaborative Islet Transplant Registry

The mission of the Collaborative Islet Transplant Registry (CITR) is to expedite progress and promote safety in islet/beta cell transplantation through the collection, analysis, and communication of comprehensive and current data on all islet/beta cell transplants performed in North America, Europe and Australia.

Age & Gender
  • 0 years ~ 99 years
  • Male, Female, Gender Inclusive
Study Interest
  • Chronic Conditions
  • Transplant
Visit Location
100% Remote (online, phone, text)
By physician referral or invitation only

Religion and Organ Donation Registration Decisions in Black Christian Communities Study

This study explores how religious beliefs influence decisions about organ donation in Black Christian communities. Many Black Americans need organ transplants, but donation rates in these communities are lower than in others. Religious beliefs may play a role in these decisions, but past research has not fully explored how people learn about their religion's views on organ donation or how these beliefs affect their choices. By interviewing Black Christians, this study aims to better understand their thoughts, experiences, and concerns about organ donation. The goal is to help create better ways to share information about organ donation that respect religious beliefs and encourage informed decision-making.

Age & Gender
  • 18 years ~ 99 years
  • Male, Female, Gender Inclusive
Study Interest
  • Healthy Volunteer or General Population
  • Minority Health
  • Opinions and Perceptions
  • Transplant
Visit Location
100% Remote (online, phone, text)
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