Breast reconstruction and neoadjuvant radiotherapy, a changing algorithm.
Recruiting
- Conditions
- breast cancermalignant neoplasm of the breast1000629110006295
- Registration Number
- NL-OMON51819
- Lead Sponsor
- niversitair Medisch Centrum Utrecht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
Women >= 18 years with:
- breast cancer
- an indication for mastectomy
- an indication for radiotherapy
- wish for a breast reconstruction
Exclusion Criteria
- Legal incapacity
- Not able to understand and sign Dutch written informed consent
- Previous history of breast cancer or another malignancy for which
radiotherapy of the breast or axilla
- Pregnant or lactating.
- Smoking
- BMI > 35 kg/m2
- cT4 tumour (and skin sparing mastectomy not possible)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary endpoint: Acute post-surgical complications at 3 months following<br /><br>mastectomy and immediate breast reconstruction after NART in the treatment of<br /><br>breast cancer. </p><br>
- Secondary Outcome Measures
Name Time Method