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Long Term Follow up of the LTOG Cohort

Long Term Follow up of the Lung Transplant Outcomes Group Cohort

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04787822
Acronym
LTOG
Enrollment
4000
Registered
2021-03-09
Start date
2021-06-15
Completion date
2027-05-31
Last updated
2026-06-03

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

Conditions

Lung Transplant Failure and Rejection

Keywords

Chronic lung allograft dysfunction, Functional status, Lung transplantation

Brief summary

The purpose of the study is to follow participants who enrolled in the Lung Transplant Outcomes Group. Clinical data, functional assessments, and surveys will be collected to determine long term graft function and functional status of lung transplant recipients.

Detailed description

This project will involve both retrospective and prospective data collection from participants enrolled in the LTOG cohort studies. We will perform long-term Chronic Lung Allograft Dysfunction (CLAD) phenotyping of lung transplant recipients who participated in the LTOG cohort studies utilizing data collected for routine clinical visits. Surviving lung transplant recipients who participated in the LTOG cohort studies will be recruited to enroll in the longitudinal portion of the project. The longitudinal component will include follow-up data collection at 6 month intervals while alive until study termination, study withdrawal, or no longer being seen for follow-up at the participating center. Follow-up data collection will include clinical data collected by study coordinators by reviewing medical records, functional assessment through administration of the Short Physical Performance Battery (SPPB), blood collection and surveys. Data from this project will be linked to data and samples collected during the LTOG cohort or ancillary studies.

Interventions

None listed

Sponsors

University of Pennsylvania
Lead SponsorOTHER
National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
Columbia University
CollaboratorOTHER
University of Alabama at Birmingham
CollaboratorOTHER
Stanford University
CollaboratorOTHER
Johns Hopkins University
CollaboratorOTHER
University of Michigan
CollaboratorOTHER
University of Pittsburgh
CollaboratorOTHER
Duke University
CollaboratorOTHER
Indiana University
CollaboratorOTHER
University of California, San Francisco
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

Long-term phenotyping of CLAD * Lung transplant recipients who have previously enrolled in the LTOG cohort studies at one of the participating centers Long-term functional status and well-being * Lung transplant recipients who have previously enrolled in the LTOG cohort studies at one of the participating centers * Alive

Exclusion criteria

Long-term phenotyping of CLAD * Lung transplant recipient not enrolled in LTOG cohort research studies Long-term functional status and well-being * Lung transplant recipient not enrolled in the LTOG cohort research studies * Lung transplant recipient not receiving post-transplant follow-up care at a participating LTOG center

Design outcomes

Primary

MeasureTime frameDescription
Chronic Lung Allograft Dysfunction (CLAD) phenotypingFrom date of transplant to the development of CLAD, up to 25 yearsChange in pulmonary function measured by serial pulmonary function tests (PFTs) and data collected at clinical care visits will be used to assess CLAD.
Functional status phenotypingFrom date of transplant to until study termination, withdrawal, or no longer being seen for follow-up at the participating center, up to 25 yearsChange in functional status will be measured by the Short Physical Performance Battery (SPPB). The SPPB is a 3-construct measure that includes gait speed, chair stands, and balance. Each construct is scored from 0 - 4 yielding an aggregate score ranging from 0 - 12. Lower SPPB scores reflect increased frailty.
Well being phenotyping-LT-VLAFrom date of transplant to until study termination, withdrawal, or no longer being seen for follow-up at the participating center, up to 25 yearsChange in well being will be measured by patient reported outcomes including the LT-VLA scale. The LT-VLA scale presents a list of activities and asks respondents to rate their difficulty in performing each one on a 4-point scale. A higher score on the LT-VLA indicates more disability.
Well being phenotyping-LT-QOLFrom date of transplant to until study termination, withdrawal, or no longer being seen for follow-up at the participating center, up to 25 yearsChange in well being will be measured by patient reported outcomes including the Lung Transplant Quality of Life (LT-QOL) survey. The Lung Transplant Quality of Life (LT-QOL) survey will be used to measure disease specific QOL. The LT-QOL utilizes 5 point scales for all items. The general quality of life scale is scored so that higher scores indicate better QOL.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJason Christie, MD

University of Pennsylvania

PRINCIPAL_INVESTIGATORScott Palmer, MD

Duke University

PRINCIPAL_INVESTIGATORJonathan Singer, MD

University of California, San Francisco

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 4, 2026