Prophylaxis With Caspofungin in High-Risk Liver Transplantation
Launched by GRUPO DE ESTUDIO DE INFECCIONES EN TRANSPLANTADOS · Jun 4, 2006
Trial Information
Current as of June 27, 2025
Unknown status
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 18 years of age or older
- • Patient has received an orthotopic liver transplantation
- • Patient meets criteria, as defined per protocol, for being considered at high risk of developing an invasive fungal infection post-liver transplantation
- • For women of childbearing potential, patient must have a negative serum or urine pregnancy test
- Exclusion Criteria:
- • Any systemic antifungal therapy (other than fluconazole for a maximum of 7 days) within 14 days of the administration of the study drug.
- • Documented (proven/probable) or suspected (possible) invasive fungal infection at the time of enrollment.
- • Abnormal laboratory values as defined per protocol.
- • Allergy, hypersensitivity, or any serious reaction to an echinocandin antifungal.
- • Patient not expected to survive at least 5 days.
- • Patient is pregnant or breast feeding.
About Grupo De Estudio De Infecciones En Transplantados
Grupo de Estudio de Infecciones en Trasplantados is a dedicated research organization focused on advancing the understanding and management of infectious diseases in transplant patients. Committed to improving patient outcomes, the group conducts rigorous clinical trials that explore innovative strategies for prevention, diagnosis, and treatment of infections that can complicate transplant procedures. By fostering collaboration among healthcare professionals and leveraging cutting-edge research methodologies, the organization aims to enhance the safety and efficacy of transplant care, ultimately contributing to the broader field of transplant medicine.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Madrid, , Spain
Valencia, , Spain
Barakaldo, Vizcaya, Spain
Barcelona, , Spain
Cordoba, , Spain
Granada, , Spain
La Coruña, , Spain
Madrid, , Spain
Madrid, , Spain
Madrid, , Spain
Malaga, , Spain
Santiago De Compostela, , Spain
Sevilla, , Spain
Patients applied
Trial Officials
Jesus Fortun, MD
Study Director
Hospital Ramon y Cajal, Madrid, Spain
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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