ISRCTN57640029
Completed
Not Applicable
Impact of implementing a surveillance of adverse events associated with totally implanted venous-access ports in cancer inpatients: a quasi-experimental study
French Ministry of Health and Sport (France)0 sites1,000 target enrollmentJanuary 13, 2011
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- French Ministry of Health and Sport (France)
- Enrollment
- 1000
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Two hospitals will participate in the study: a university hospital, and a hospital exclusively dedicated to the care of cancer patients. In each hospital, wards performing cancer intravenous chemotherapy as a usual activity will be approached and proposed the implementation of a surveillance of adverse events associated with totally implanted venous\-access ports. Only patients (male or female adults above 18 years old) with totally implanted venous\-access ports used for cancer chemotherapy will be included in this surveillance.
Exclusion Criteria
- •Wards with no, or infrequent, activity of cancer chemotherapy will not be included in the study. In wards participating in the study, patients with totally implanted venous\-access ports used for other treatment than cancer chemotherapy (antibiotics, parenteral nutrition, etc.) will not be included in the surveillance.
Outcomes
Primary Outcomes
Not specified
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