Voriconazole as Prophylactic Therapy in Lung Transplant Recipients
Stopped early · Phase 4
Conditions studied: Infection
In brief
The purpose of this study is to compare the safety and efficacy of Voriconazole with Itraconazole following lung transplantation.
Key facts
- Study ID
- NCT00455364
- Run by
- University of Chicago
- People needed
- 20
- Starts
- 2007-04-01
- Expected to finish
- 2007-04-01
- Last updated by the study team
- 2013-02-06
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Bilateral-lung or single-lung transplant recipients between the ages of 18- 65 years old.
- Patients must be able to give informed consent prior to and again after transplantation
You may not qualify if…
- Lung transplant patients unable to give informed consent.
- Prior adverse reaction to the drug itraconazole or voriconazole
Where it is running
- The University of Chicago — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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