Clinical trial · Interventional
Pilot Study Evaluating a Perioperative E-follow-up Protocol in Patients With Ambulatory Surgery for Breast Cancer
NCT03289286CI-TRIAL-00034148PITCAcompletedN/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)
This is a monocentric, prospective cohort study evaluating the feasibility of a perioperative e-follow-up protocol in patients with ambulatory surgery for breast cancer. This protocol will be based on: * A coordinated ambulatory follow-up performed by a dedicated nurse * An electronic follow-up tool used in pre- and post-surgery Patients will be followed 8 days before the surgery until 30 days after the surgery of breast cancer.
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 Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Dedicated and coordinated e-follow-up. | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- OTHER
- label
- Patients with breast cancer operated in ambulatory
- interventionNames
- Other: Dedicated and coordinated e-follow-up.
Primary outcomes (1)
- measure
- Rate of patients without failure to the e-follow-up. A failure is defined by absence of connection to the electronic tool and the mismatch between the alert level and severity of complications.
- timeFrame
- 1.5 months by patient
Secondary outcomes (5)
- measure
- Patient satisfaction to the e-follow-up.
- timeFrame
- 1.5 months by patient
- description
- Satisfaction will be evaluated by questionnaire.
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patient eligible for an ambulatory surgery of breast cancer (partial mastectomy with or without lymph node sampling) 2. Ambulatory surgery planned 10 days or more after inclusion date 3. Age \> or = 18 years old 4. Affiliated to the french social security system 5. Patient must provide written informed consent prior to any study-specific procedure or assessment Exclusion Criteria: 1. Surgery other than breast cancer surgery in ambulatory (benign breast surgery, other surgical specialities) 2. Patient who cannot connect to the electronic tool at home (no computer, no tablet computer or no internet connection) 3. Pregnant or breastfeeding women 4. Any psychological, familial, geographic or social situation, according to the judgment of investigator, potentially preventing the provision of informed consent or compliance to study procedure 5. Patient protected by law
References
Publications (0)
Data not yet available
No reference posted for this study.