Informations générales (source: ClinicalTrials.gov)

NCT00274885 Statut inconnu
Study of the Relationship Between the Rate of Residual Platinum in the Blood and the Incidence of Persistent Neurotoxicity in Patients Treated for Gastrointestinal Cancer With Oxaliplatin
Interventional
  • Tumeurs gastro-intestinales
  • Syndromes neurotoxiques
Phase 4
GERCOR - Multidisciplinary Oncology Cooperative Group (Voir sur ClinicalTrials)
octobre 2005
29 juin 2024
RATIONALE: Learning about the relationship between platinum levels in the blood and neurotoxicity in patients receiving oxaliplatin may help plan treatment and may help patients live more comfortably. PURPOSE: This phase IV trial is studying the relationship between platinum levels in the blood and neurotoxicity in patients who are receiving oxaliplatin for gastrointestinal cancer.
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Etablissements

Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
AP-HP - Hôpital La Pitié-Salpêtrière Jean-Baptiste Meric, MD En recrutement IDF Contact (sur clinicalTrials)
AP-HP - Hôpital Saint Antoine Olivier Rosmorduc, MD, PhD En recrutement IDF Contact (sur clinicalTrials)
AP-HP - Hôpital Tenon Thierry Andre, MD En recrutement IDF Contact (sur clinicalTrials)
Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Centre Hospital Universitaire Hop Huriez - 59037 - Lille - France Mohamed Hebbar, MD En recrutement Contact (sur clinicalTrials)
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
CHU de Grenoble - Hopital Michallon - 38043 - Grenoble - France Christine Rebischung En recrutement Contact (sur clinicalTrials)
Clinique Saint Jean - 69008 - Lyon - France Gerard Lledo En recrutement Contact (sur clinicalTrials)

Critères

Tous
DISEASE CHARACTERISTICS:

- Diagnosis of gastrointestinal cancer

- Receiving or planning to receive 8 months of oxaliplatin-based chemotherapy

- No pre-existing neuropathy

- No CNS disease or cerebral metastases

PATIENT CHARACTERISTICS:

- WHO 0-1

- Life expectancy ≥ 12 weeks

- No biliary or gastro-duodenal obstruction

- No familial, social, geographical, or psychological condition that would preclude
study treatment

PRIOR CONCURRENT THERAPY:

- See Disease Characteristics

- No other concurrent drug or agent that is potentially neurotoxic