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TRANSPIRE: Lung Injury in a Longitudinal Cohort of Pediatric HSCT Patients

TRANSPIRE: Lung Injury in a Longitudinal Cohort of Pediatric HSCT Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04098445
Enrollment
2000
Registered
2019-09-23
Start date
2021-09-08
Completion date
2033-09-01
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchiolitis Obliterans, Diffuse Alveolar Hemorrhage, Hematopoietic Stem Cell Transplant (HSCT), Interstitial Pneumonitis, Thrombotic Microangiopathies

Brief summary

Hematopoietic stem cell transplant (HSCT) is an effective but toxic therapy and pulmonary morbidity affects as many as 25% of children receiving transplant. Early pulmonary injury includes diffuse alveolar hemorrhage (DAH), thrombotic microangiopathy (TMA) interstitial pneumonitis (IPS) and infection, while later, bronchiolitis obliterans is a complication of chronic GVHD associated with severe morbidity and mortality. Improved diagnosis and treatment of pulmonary complications are urgently needed as survival after HSCT improves, and as HSCT is increasingly used for non-malignant disorders such as sickle cell disease. Currently, there are large and important gaps in the investigator's knowledge regarding incidence, etiology and optimal treatment of pulmonary complications. Moreover, young children unable to perform spirometry are often diagnosed late, and strategies for monitoring therapeutic response are limited. This is a prospective multi-institutional cohort study in pediatric patients undergoing allogeneic hematopoietic stem cell transplantation (alloHSCT). Assembly of a large prospective uniformly screened cohort of children receiving HSCT, together with collection of biological samples, will be an effective strategy to identify mechanisms of lung injury, test novel diagnostic strategies for earlier diagnosis, and novel treatments to reduce morbidity and mortality from lung injury after transplant.

Interventions

None listed

Sponsors

Children's Hospital Medical Center, Cincinnati
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 24 Years
Healthy volunteers
No

Inclusion criteria

* Subjects ≤ 24 years of age undergoing allogeneic or autologous HSCT.

Exclusion criteria

* Subjects over 24 years of age.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of Lung Injury after HSCT24 months after HSCTParticipants will be assessed for lung injury at 24 months after HSCT

Countries

United States

Contacts

CONTACTStephanie Edwards, BSN, RN
StephanieL.Edwards@cchmc.org513-636-9292
PRINCIPAL_INVESTIGATORStella Davies, MBBS, PhD, MRCP

Children's Hospital Medical Center, Cincinnati

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 1, 2026