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Search / Trial NCT00333645

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

Liver Transplantation Invasive Fungal Infection Invasive Aspergillosis Prophylaxis Caspofungin

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.

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

0 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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