Bone Marrow Transplant

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Review clinical trials related to Bone Marrow Transplant. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Shingrix In Recipients of Allogeneic Transplants

This research is designed to determine if the adjuvanted recombinant glycoprotein E (gE) herpes zoster (HZ) vaccine (Shingrix) has acceptable immunogenicity and safety in people who have undergone allogeneic stem cell transplant (allo-SCT). Specifically, it will determine the effect of the interval after transplantation on the immune response and if an additional dose of vaccine is needed to improve the vaccine-induced responses.

Participants needed: 55
Trial details
Phase: Phase 2Age: 18-79Biological sex: AllType: InterventionalSponsor: University of Colorado, DenverUpdated: Feb 5, 2026Locations: 1
Eligibility criteria

Allo-SCT recipients being age 18 - 79 years at time of allo-SCT. [+7]

Active Graft Versus Host Disease (aGVHD) at the time of enrollment and receipt o... [+7]

Status: Recruiting

Activity Levels in Bone Marrow Transplant Patients

Participants in this study will be receiving a bone marrow transplant. This study is designed to evaluate correlations between activity levels and length of stay, quality of life, and hand grip strength.

Participants needed: 200
Trial details
Age: 18-99Biological sex: AllType: ObservationalSponsor: Michael TomassonUpdated: Nov 10, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Cardiovascular Risk in Children With Chronic Conditions Study

Children living with chronic health conditions face a higher risk of developing cardiovascular diseases than their peers, largely due to the accelerated aging of the heart and blood vessels. Although experts recognize this elevated risk and recommend close monitoring and early intervention, the underlying mechanisms driving this phenomenon remain poorly understood. At present, no effective interventions specifically target its root causes. Recent research shows that both large blood vessels (such as the carotid artery) and small vessels (such as those in the retina) can display early signs of damage decades before clinically apparent heart or vascular disease emerges. This accelerated vascular aging can result from multiple factors - including disease-related processes such as persistent inflammation and metabolic disturbances, treatment-related effects such as chemotherapy or long-term steroid use, and lifestyle changes associated with chronic illness, such as reduced physical activity and altered eating habits. However, it is still unclear how these factors influence the development and progression of vascular changes in children as they grow. Importantly, these changes can be monitored through non-invasive methods, offering a unique opportunity to study at-risk patients many years before overt cardiovascular disease develops. Identifying these early changes may enable us to detect and track individuals at heightened risk well in advance of clinical disease. This study aims to deepen our understanding of the causes of increased cardiovascular risk in children with chronic conditions and to lay the groundwork for earlier, more targeted prevention strategies.

Participants needed: 300
Trial details
Age: 6-25Biological sex: AllType: ObservationalSponsor: Semmelweis UniversityUpdated: Aug 8, 2025Locations: 3
Eligibility criteria

Individuals aged between 6 and 25 years; [+2]

Severe intellectual and developmental disability; [+5]

Status: Recruiting

Mosaic Trial for Stem Cell Transplant Recipients

The goal of this clinical trial is to learn if using an intervention website (Mosaic) improves selected patient-reported outcomes in adult blood cancer patients undergoing allogeneic or autologous stem cell transplant, compared to using an educational website (control group). Patients will be recruited prior to their scheduled transplant, then randomized to use one of these two study websites throughout the study. They will complete five assessments during the study: one before transplant (baseline) and four after transplant (2, 4, 6, and 8 month follow-ups). The main questions this trial aims to answer are: 1. Compared to patients using the control group website, do patients using the intervention website report greater improvements in general psychological distress, cancer treatment-related distress, physical symptoms, and health-related quality of life? 2. Are these benefits at least partially explained by improvements in perceived preparedness, self-efficacy, and approach coping and/or reductions in avoidant coping and perceived stress? 3. Do some patients benefit more from using the intervention website than others? Specifically, we will examine whether patients' primary language (English/Spanish) and their initial psychological distress are related to the benefit they get from using the intervention website. We will also explore effects of sex, race, ethnicity, and transplant type.

Participants needed: 356
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northwestern UniversityUpdated: Jul 18, 2025Locations: 3
Eligibility criteria

Diagnosed with a hematologic cancer according to medical records [+5]

Currently participating in a behavioral intervention targeting distress, health-... [+2]