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Imatinib Concentration Monitoring Evaluation
Why monitoring in the scope of a study?
Practical information
Study documents
Contact & investigators
Related publications
Abstracts

pcl.info@chuv.ch


Study documents: Imatinib Concentration Monitoring Evaluation (I-COME)

A Study to Compare the Clinical Usefulness of «Routine» versus «Rescue» Therapeutic Drug Monitoring (TDM) Interventions in Chronic Myeloid Leukemia (CML) Patients

You can find below every documents related to this study:

      1. Study summary & information to recruiting physicians:

English Français Deutsch

Italiano

PDF Summary PDF Résumé PDF Übersicht
PDF Presentation (slides) PDF Lettre d'information PDF Informationsbrief PDF Lettera d'informazione

The study has been approved by local Ethics Committees for the following Swiss cantons: see Approval paragraph.

      2. Inclusion documents:

a) Blood measurement request form (serving as case reprot form, CRF)

PDF Bon de demande de dosage / Formular zur Plasmaspiegelmessung

b) Patient information & consent form

Français Deutsch Italiano
PDF Information aux patients PDF Patienteninformtation PDF Informazione per i pazienti
PDF Consentement PDF Einverständniserklärung PDF Consenso informato

c) Invoice example (for administrative work associated with the study)

PDF Facture-type     PDF Rechnungsvorlage

Contact

Verena Gotta
I-COME coordinator
Division of Clinical Pharmacology and Toxicology
Centre Hospitalier Universitaire Vaudois – CHUV
1011 Lausanne – SWITZERLAND

tel.: +41 21 314 42 69 e-mail: info@imatinib-monitoring.ch
fax.: +41 21 314 42 66 website: www.imatinib-monitoring.ch


Dernière modification le 02.11.2010 - Impressum - Informations juridiques