Actively Recruiting

Age: 18Years +
All Genders
ID04664192

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

Led by Baylor Research Institute · Updated on 2026-01-30

100

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying advanced lung diseases, including lung transplantation care, to better understand the effects of viral and other infectious exposures on lung transplant and chronic lung disease patients. The study supports biomarker research to identify specific indicators in blood or tissue that can help in early diagnosis and personalized treatment for conditions like interstitial lung disease, chronic obstructive lung disease (COPD), and post-lung transplant rejection. Participants are observed through a biobank registry focused on lung transplant recipients. Clinical data and blood samples are collected during visits to support research on genetic risk, infectious disease susceptibility, and structural lung disease. This observational study gathers human biological specimens to advance understanding, diagnosis, and treatment of chronic lung diseases and improve post-lung transplant care. During the study, participants provide blood samples and clinical data at regular visits. Researchers track patient diagnoses and survival over five years to assess outcomes related to lung transplantation. The collected information helps evaluate biomarkers and genetic factors linked to disease progression and therapy response. Participants are monitored for long-term outcomes, contributing to ongoing research in lung health and transplant success.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be 18 years of age or older
  • Have undergone lung transplantation at Baylor University Medical Center within the past 10 years
  • Be able to understand and sign the informed consent form
Not Eligible

You will not qualify if you...

  • Have significant documented anemia with hemoglobin less than 8 g/dL
  • Have had blood transfusions within the past 3 weeks
  • Have active cancer (excluding skin cancers)
  • Enrollment is against doctor recommendation
  • Unable to provide informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 5 years

Participants are observed through periodic blood sample collections to support research on lung transplant outcomes.

Periodic blood sample collection visits

Trial Site Locations

Total: 1 location

1

Baylor Scott & White Research Institute

Dallas, Texas, United States, 75246

Actively Recruiting

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Research Team

S

Susan Mathai, MD

T

Tammy Fischer

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

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