Clinical trial · Observational
Assessment of Complications, Quality of Life and Easiness of Use of Implantable Central Venous Access Ports
Assessment of Complications, Quality of Life and Easiness of Use of Implantable Central Venous Access Ports : Cohort and Prospective Study
NCT00921141CI-TRIAL-00007528CCIcompletedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a prospective, descriptive and observational study of the anticancer center practice
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (1)
- label
- study population
- description
- Patient with cancer requiring a long-term central venous catheter
Primary outcomes (1)
- measure
- Incidence and collection of complications for the patients requiring an implantable central venous access ports substitution/change
- timeFrame
- Until the implantable central venous access ports removal
Secondary outcomes (3)
- measure
- Brief description of the different risk factor for morbidity
- timeFrame
- Until the implantable central venous access ports removal
- measure
- Assessment of the implantable central venous access ports ease-of-use for nurses according to the modalities of implementation and patient features
- timeFrame
- Until the implantable central venous access ports removal
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patient with any cancer, requiring a central venous catheter * No contraindication for any surgery with local or complete anaesthesia Exclusion Criteria: * Previous Xylocaine or Lidocaine allergy * Clinic superior vena cava syndrome
References
Publications (0)
Data not yet available
No reference posted for this study.