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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00284726
Other study ID # 00-10-25-03
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date December 2000
Est. completion date September 2005

Study information

Verified date December 2017
Source Johns Hopkins University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare 2 different cold storage solutions, used to preserve donor lungs for lung transplantation, and their effect on cytokine activation related to ischemic reperfusion injury. Primary endpoint is 30 day survival.


Description:

The length of ischemic time in harvesting lung allografts is associated with graft survival. It is further thought that ischemic changes in early post-transplantation bronchoscopic biopsies has a direct correlation with later development of chronic rejection.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date September 2005
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: Any patient undergoing a lung trasnplant at Johns Hopkins Hospital - Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Celsior Cold Storage Solution


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Johns Hopkins University
See also
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Recruiting NCT03873597 - Physical Activity Tele-coaching in Lung Transplant Recipients N/A