EvaLuating negAtive pressUre wound theRapy in brEast coNserving surgery - the LAUREN pilot study
Recruiting
- Conditions
- breast cancermammacarcinoma10006291
- Registration Number
- NL-OMON53621
- Lead Sponsor
- Zuyderland Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 300
Inclusion Criteria
- Eighteen years or older.
- Female sex.
- Indication for breast conserving surgery, with or without sentinel lymph node
biopsy
Exclusion Criteria
- Undergoing mastectomy or modified radical mastectomy.
- Undergoing direct breast reconstruction.
- Patients with a pacemaker, ICD or other medical device in the proximity of
the wound area, due to the magnet in the PICO® device.
- Unable to comprehend implications and extent of the study and/or unable to
sign for informed consent.
- Participation in another breast cancer surgery related clinical trial.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method