Clinical trial · Interventional
Feasibility Assessment of a Patients Follow-up Visit Receiving Trastuzumab Subcutaneous by Advanced Practice Nurse
Feasibility Assessment of a Patients Follow-up Visit Receiving Trastuzumab Subcutaneous by Advanced Practice Nurse - TIPA
NCT02686918CI-TRIAL-00021007TIPAunknownN/AClinicalTrials.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)
The main of this study is to assess the feasibility of a patients follow-up visit receiving trastuzumab subcutaneous by Advanced Practice Nurse.
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 |
|---|---|---|---|
| Breast Neoplasms | Breast Neoplasm | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Advanced Practice Nurse consultation | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- consultation by Advanced Practice Nurse.
- description
- During consultations, patients will be seen successively by Advanced Practice Nurse and referent oncologist.
- interventionNames
- Other: Advanced Practice Nurse consultation
Primary outcomes (1)
- measure
- Percentage of consultation requiring a medical advice between IPA and oncologist
- timeFrame
- 1 year
- description
- Estimate the correlation between the IPA and the oncologist about whether or not a medical opinion during the consultation
Secondary outcomes (2)
- measure
- Percentage of consultations delegated to the IPA
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patient care at the Cancer Institute Lucien Neuwirth * Patient aged over 18 years * Patient with breast cancer overexpressing HER2 adjuvant * Patient having finished their chemotherapy treatment with IV followed the oncologist day hospital * Patient under Trastzumab subcutaneously * Patient affiliated or entitled to a social security scheme (mandatory requirement for all studies) Exclusion Criteria: * Refusal to participate, most patient protected under guardianship. * Patient in inability to understand the course of the study * Patient with documented history of cognitive or psychiatric disorders. * Patients pregnant or lactating * Patients under guardianship or curatorship
References
Publications (0)
Data not yet available
No reference posted for this study.