Actively Recruiting
Magseed Pro(R)/ Sentimag(R) Gen3
Led by Endomagnetics Ltd. · Updated on 2024-09-19
224
Participants Needed
6
Research Sites
173 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to provide prospective evidence that the Magseed Pro® marker /Sentimag® Gen3 system is safe and effective for marking A. suspicious/biopsy-proven positive axillary lymph nodes; and B. soft tissue lesions including cancer and pre-cancerous change in the breast
CONDITIONS
Official Title
Magseed Pro(R)/ Sentimag(R) Gen3
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant is willing and able to give informed consent for participation in the study
- Participant is aged 18 years or older at the time of consent.
- Patients requiring breast lesion or axillary node marking and excision
You will not qualify if you...
- Pregnant or nursing subjects and those planning pregnancy during the study follow-up period
- Presence of other medical, social, or psychological conditions that may limit participation or compliance
- Known hypersensitivity to Nitinol
- Current active infection at the breast implantation site
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 6 locations
1
Marienhospital Bottrop GmbH
Bottrop, Germany
Actively Recruiting
2
AGAPLESION Markus Frankfurter Diakonie Kliniken gGmbH
Frankfurt, Germany
Actively Recruiting
3
Technical University Munich
Munich, Germany
Not Yet Recruiting
4
Guy's Hospital
London, United Kingdom
Actively Recruiting
5
Royal Marsden Hospital
London, United Kingdom
Actively Recruiting
6
University Hospital South Manchester
Manchester, United Kingdom
Actively Recruiting
Research Team
M
Matt Womack, Dr
CONTACT
T
Tanja Odeneg, Dr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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