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Lung Transplantation Study Among Prospective Observational Solid Organ Transplantation Studies

Establishment and operation of long-term transplant cohorts: Lung Transplant Cohort

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0010411
Enrollment
630
Registered
2025-04-11
Start date
2015-03-29
Completion date
Unknown
Last updated
2025-05-07

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

Conditions

None listed

Interventions

None listed

Sponsors

Yonsei University Health System, Severance Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subject inclusion criteria: - If you agree to participate in the study before transplant surgery or if you have received a pancreas transplant from January 2015 until the time of institutional IRB approval(consent is exempt for those subjects due to retrospective data collection) - Age 19 or older at the time of transplant surgery - However, if a consent from for retrospective study subject follow-up is received, it is included in prospective data collection from the time after obtaining the consent from.

Exclusion criteria

Exclusion criteria: Multiple organ transplantation (including simultaneous cardiac and lung transplantation)

Design outcomes

Primary

MeasureTime frame
Death;rejection requiring treatment;transplant organ loss;retransplantation;loss to follow-up combined endpoint

Secondary

MeasureTime frame
Death: Death due to cardiovascular disease or unknown death due to other causes;Occurrence of acute rejection reaction;Occurrence of transplant angiopathy;Diabetes after transplantation;Occurrence of infection after transplantation;Occurrence of malignant tumor after transplantation;Occurrence of chronic kidney disease after transplantation;Occurrence of musculoskeletal complication after transplantation

Countries

Korea, Republic of

Contacts

Public ContactJin Gu Lee

Yonsei University

csjglee@yuhs.ac+82-2-2228-2140

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026