Study of Lung Injury Over Time in Children and Young Adults Undergoing Hematopoietic Stem Cell Transplant
Led by Children's Hospital Medical Center, Cincinnati · Updated on 2026-06-22
2000
Participants Needed
9
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Researchers are studying lung injury in children and young adults who receive hematopoietic stem cell transplants HSCT. This study aims to better understand lung complications such as diffuse alveolar hemorrhage, thrombotic microangiopathy, interstitial pneumonitis, and bronchiolitis obliterans that affect many patients after HSCT. Since HSCT is increasingly used for non-cancer conditions like sickle cell disease, improving diagnosis and treatment of lung problems is important to reduce illness and death.
This is a prospective, multi-center observational study involving pediatric and young adult patients undergoing allogeneic or autologous HSCT. The study collects biological samples and uniformly screens participants over time to identify causes of lung injury and evaluate new diagnostic methods and treatments. Participants are followed for lung injury incidence up to 24 months after their transplant.
During the study, participants undergo regular assessments to monitor lung health. Researchers collect data on lung injury occurrence and progression, aiming to understand and improve outcomes after HSCT. The primary measurement is the incidence of lung injury within two years following transplant. The study runs from September 2021 to September 2033, providing long-term observation of lung complications in this population.
CONDITIONS
Brief Title
TRANSPIRE: Lung Injury in a Longitudinal Cohort of Pediatric HSCT Patients
Research Team
S
Stephanie Edwards, BSN, RN
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match. Sign up to get personalized trial recommendations delivered to your inbox.
Subjects 24 years of age or younger undergoing allogeneic or autologous hematopoietic stem cell transplantation
You will not qualify if you...
Subjects over 24 years of age
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Similar Trials
Study of Belumosudil With or Without Standard Care for New and Early Bronchiolitis Obliterans Syndrome After Stem Cell Transplant
Pilot Study of Bronchial Epithelium Changes in Children Aged 1 Month to 6 Years With Post-infectious Bronchiolitis Obliterans After Adenovirus or Rhinovirus Infection
Study of Complement Defects in Thrombotic Microangiopathy and Related Conditions Including Severe Hypertension Using the HMEC Test
Building a Patient Database for Thrombotic Microangiopathies
Collecting Clinical Data on TMA Patients
Study of Immunosuppression, Caplacizumab, and Plasma Infusion Without Plasma Exchange in Adults With Immune-Mediated Thrombotic Thrombocytopenic Purpura
Phase 2 Study of Narsoplimab Treatment in Children 28 Days to Under 18 Years With High-Risk Hematopoietic Stem Cell Transplant Thrombotic Microangiopathy
Study of Clonogenic Epithelial Cells in Patients with Bronchiolitis Obliterans Syndrome After Stem Cell or Lung Transplant
Identifying Plasma Biomarkers for Early Detection of Transplant-associated Thrombotic Microangiopathy
Using Proteomics and Metabolomics in Patients Undergoing Stem Cell Transplantation
Study of Ivosidenib as Maintenance Treatment After Stem Cell Transplant in Adults with IDH1-Mutant Acute Myeloid Leukemia
Observational Study of Thrombosis and Hemostasis Diseases in Chinese Patients
Tracking Causes, Treatments, Outcomes, and Costs
Have more questions? Get in touch with our team for quick support
Published Research Related To This Trial
High Prevalence of Abnormal Baseline Lung Function in Pediatric and Young Adult Hematopoietic Stem Cell Transplant Recipients: A Report from the TRANSPIRE Study.