NCT02167490Active, not recruiting
Sentinel Node Vs Observation After Axillary Ultra-souND
A Randomized Trial Comparing Sentinel Lymph Node Biopsy Vs no Axillary Surgical Staging in Patients With Small Breast Cancer and a Negative Preoperative Axillary Assessment (IEO S637/311)
Source: ClinicalTrials.gov · Last updated 25 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The hypothesis of this trial are that: * avoiding axillary surgery does not worsen the outcome of patients with small breast cancer the absence of the pathological information on the risk of recurrence given by nodal status is not worsening outcome of these patients * pre-operative imaging of the axilla can identify patients with clinically relevant nodal burden. The aims of this prospective randomized study are: * to verify whether, in presence of a negative preoperative axillary assessment, SLN can be spared * to verify whether, in presence of a negative preoperative axillary assessment, the decision on adjuvant medical treatment can be taken according only to the biology of the tumour without the prognostic information achieved by SLNB on the nodal status * to verify whether, in presence of a negative preoperative axillary assessment, the patients' quality of life can be improved by a less invasive surgical procedure.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 1560 (estimated)
- First submitted
- 18 Apr 2014
- Start date
- 1 Jan 2012
- Primary completion date
- 30 Jun 2025
- Lead sponsor
- European Institute of Oncology
- Diseases
- Childhood cancers
- NCT number
- NCT02167490
What you commit to
- Study type: Interventional
- Planned participants: 1560
- From 1 Jan 2012 to the primary completion date, 30 Jun 2025
- 18 sites in 4 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- previous primary systemic therapy
Other illness
- previous malignancy
- bilateral breast cancer
- multicentric or multifocal breast cancer
- patients with psychiatric, addictive, or any disorder, which compromises ability to give informed consent for participation in this study.
Other
- synchronous distant metastases
- pregnancy or breastfeeding
- pre-operative diagnosis (cytology or histology) of axillary lymph node metastases
- pre-operative radiological evidence of multiple involved or suspicious nodes
Who the study is looking for
- breast cancer \<2 cm, and a clinically negative axilla
- any age
- candidates to receive breast conserving surgery + radiotherapy
- negative preoperative assessment of the axilla (ultra-sound with or without FNAC in case one doubtful node is found)
- written informed consent must be signed and dated by the patient and the investigator prior to inclusion.
- patients must be accessible for follow-up.
Sex: Female · Does not accept healthy volunteers
Sites (18)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Universitätsspital Bern Klinik und Poliklinik für Medizinische Onkologie Coordinator of this site? Confirm its status | Bern | Switzerland | Unknown status |
| Instituto Oncologico Fundacion Arturo Lopez Perez Coordinator of this site? Confirm its status | Santiago | Chile | Unknown status |
| Health Research Institute Hospital La Fe Coordinator of this site? Confirm its status | Valencia | Spain | Unknown status |
| Comprensorio Sanitario Coordinator of this site? Confirm its status | Bolzano | Italy | Unknown status |
| Azienda Ospedaliera Spedali Civili Coordinator of this site? Confirm its status | Brescia | Italy | Unknown status |
| Ospedale Oncologico Regionale Coordinator of this site? Confirm its status | Cagliari | Italy | Unknown status |
| Humanitas Mater Domini Coordinator of this site? Confirm its status | Castellanza | Italy | Unknown status |
| Ospedale S. Anna Coordinator of this site? Confirm its status | Como | Italy | Unknown status |
| Azienda Ospedaliera Carlo Poma Coordinator of this site? Confirm its status | Mantua | Italy | Unknown status |
| Fondazione IRCCS Istituto Nazionale Tumori Coordinator of this site? Confirm its status | Milan | Italy | Unknown status |
| European Institute of Oncology Coordinator of this site? Confirm its status | Milan | Italy | Unknown status |
| Istituto Nazionale Tumori Coordinator of this site? Confirm its status | Naples | Italy | Unknown status |
| AOU Federico II Coordinator of this site? Confirm its status | Naples | Italy | Unknown status |
| Ospedale San Matteo Coordinator of this site? Confirm its status | Pavia | Italy | Unknown status |
| Ospedale Guglielmo di Saliceto Coordinator of this site? Confirm its status | Piacenza | Italy | Unknown status |
| Ospedale Fatebenefratelli Coordinator of this site? Confirm its status | Roma | Italy | Unknown status |
| Humanitas Cancer Center Coordinator of this site? Confirm its status | Rozzano | Italy | Unknown status |
| Ospedale S. Anna Coordinator of this site? Confirm its status | Torino | Italy | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.