An observational study in Cancer, sponsored by Centre Oscar Lambret. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-07-23.
Sponsored by Centre Oscar Lambret · Observational
This is a prospective, descriptive and observational study of the anticancer center practice
Centre Oscar Lambret is the lead sponsor of 127 studies on the registry; 13 are open to participants now.
Counted across the registry records on this site, refreshed daily.
All the patients requiring the implementation of a catheter in an anticancerous center
Exclusion Criteria:
Patient with cancer requiring a long-term central venous catheter
Incidence and collection of complications for the patients requiring an implantable central venous access ports substitution/change
Time frame: Until the implantable central venous access ports removal
Brief description of the different risk factor for morbidity
Time frame: Until the implantable central venous access ports removal
Assessment of the implantable central venous access ports ease-of-use for nurses according to the modalities of implementation and patient features
Time frame: Until the implantable central venous access ports removal
Assessment of the patient quality of life
Time frame: Before central venous access ports implementation, at the first day of chemotherapy, and during the cycle 4 of chemotherapy
This study is completed, as verified in Jul 2012. You cannot join it, but the record below documents what was studied.
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Centre Oscar Lambret