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Bio-Banking of Specimens for Advanced Lung Disease and Lung Transplant Research

Bio-Banking of Specimens for Advanced Lung Disease and Lung Transplant Research

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04664192
Acronym
ALD Biobank
Enrollment
100
Registered
2020-12-11
Start date
2021-06-04
Completion date
2027-01-01
Last updated
2026-08-13

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

Conditions

Interstitial Lung Disease, Lung Diseases, Respiratory Failure

Brief summary

A major goal of this protocol is to support biomarker studies in advanced lung diseases, lung transplantation care, and to improve our understanding of the effects of viral and other infectious exposures to outcomes in our lung transplant and ALD patient populations.

Detailed description

The identification of biomarkers in a patient's blood or tissue that are specific for particular medical conditions (such as interstitial lung disease, chronic obstructive lung disease (COPD), and post-lung transplant rejection) is important for the prevention and early detection of the disease, as well as to advance our understanding of targeted therapies. Availability of biomarkers for diagnosis and for the prediction of patient prognosis and therapy promises personalized medicine. Patients may be selected based on the presence of particular gene mutations or circulating protein levels to receive personalized treatment. Furthermore, knowledge regarding genetic risk and susceptibility to infectious diseases as well as structural lung disease is rapidly growing-as whole genome sequencing and genome-wide association studies have become easier to do, genetic risk has emerged as increasingly important in understanding why and how some patients develop chronic lung disease. This is true for the spectrum of lung diseases treated in the ALD program, from those with airways diseases such as COPD to diffuse parenchymal lung diseases such as idiopathic pulmonary fibrosis (IPF). The availability of human biological specimens for research purposes is crucial for the advancement of medical knowledge of understanding, diagnosing, and treating chronic lung diseases and optimizing post-lung transplant care.

Interventions

OTHERPatient Biospecimen Registry (observational and blood sampling)

Clinical data collected at every blood sample collection visit.

Sponsors

Baylor Research Institute
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. All individuals aged 18 years and older 2. Persons who have undergone lung transplantation at Baylor University Medical Center in the previous 10 years 3. Individual is able to understand and sign the informed consent form

Exclusion criteria

1. Significant documented anemia (hemoglobin \<8 g/dL) 2. Blood transfusions within past 3 weeks 3. Active cancer (non-skin cancers) 4. Enrollment against doctor recommendation 5. Patient not able to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Diagnosis of patients with lung transplant5 yearsICD 10 code for underlying lung disease

Secondary

MeasureTime frameDescription
Survival5 yearsDate of death

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORSusan Mathai, MD

Baylor Scott & White Research Institute

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 14, 2026