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Search / Trial NCT02279121

ATAPAC Study (TauroLock Activity in Adult Cancer Patients)

Launched by CENTRE HOSPITALIER RÉGIONAL METZ-THIONVILLE · Oct 29, 2014

Trial Information

Current as of June 15, 2025

Completed

Keywords

Central Venous Catheter Taurolidine Lock Therapy

ClinConnect Summary

The central venous catheter (CVC)-associated bloodstream infection (CLABSI) represent a serious and persistent health problem in cancer patients with an implantable CVC receiving an intravenous (IV) anti-tumor therapy. The CLABSI include the CVC-associated bacteremia and the negative bloodstream local or generalized infections. CLABSI significantly increase morbidity and hospital costs. They can lead also to discontinuation of IV anti-tumor treatment, a severe sepsis, a septic shock or a death. Microbial colonization and biofilm development, which are resistant to antibiotic therapy, often ...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients older than 18 years
  • Performance Index (WHO score) ≤ 2
  • Patient with a solid cancer receiving an IV anti-tumor treatment
  • Presence of a totally implantable CVC
  • Anti-tumoral therapy administered by a totally implantable CVC
  • Metastatic and / or (neo) adjuvant treatment
  • Full hospitalised and / or day-hospital patients
  • Informed written consent
  • Social Health security insurance
  • Exclusion Criteria:
  • Hematological cancer patients
  • HIV-positive patients and/ or patients receiving an active immunosuppressive therapy
  • Patients presenting a febrile episode within 4 days prior to randomisation
  • Patients with neutropenia grade ≥ 2 (ANC ≤ 1000/mm3) on a blood testing older than 7 days
  • Patients on IV antibiotic therapy
  • Patients on total and / or peripheral parental nutrition
  • Patients with a previous CLABSI history
  • Allergy to citrate or taurolidine
  • Patients who are not able to give an informed consent
  • Patients under guardianship
  • Patients under judicial protection
  • Pregnant or breastfeeding woman

About Centre Hospitalier Régional Metz Thionville

The Centre Hospitalier Régional Metz-Thionville is a leading healthcare institution in the Grand Est region of France, dedicated to delivering high-quality medical care and advancing clinical research. With a multidisciplinary team of experienced healthcare professionals, the center emphasizes patient-centered services and innovative treatment approaches. Committed to enhancing medical knowledge and improving patient outcomes, the hospital actively participates in clinical trials across various therapeutic areas, fostering collaboration with academic institutions and industry partners to drive advancements in healthcare.

Locations

Metz, , France

Patients applied

0 patients applied

Trial Officials

Raffaele LONGO, MD

Principal Investigator

CHR Metz Thionville

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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