Actively Recruiting
Quality of Life After Breast Cancer Surgery
Led by Centre Hospitalier de Colmar · Updated on 2025-09-08
1500
Participants Needed
1
Research Sites
521 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational study is to prospectively collect data on quality of life after oncoplastic breast surgery. Participants will be followed-up and answer quality of life questionnaire for a duration of 5 years after surgery.
CONDITIONS
Official Title
Quality of Life After Breast Cancer Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient aged 18 or over
- Patient with breast cancer of any stage (including in situ) or healthy individual at high personal risk
- Patient requiring breast surgery under general anesthesia for therapeutic or prophylactic purposes
- Patient capable of complying with study requirements in the investigator's opinion
- Patient with a computer, tablet, or smartphone connected to the Internet
- Patient followed regularly at the center according to standard recommendations
You will not qualify if you...
- Patient requiring surgical intervention under local anesthesia only
- Patient requiring surgery only for installation or removal of a chemotherapy implantable port
- Patient with a history of cancer other than breast cancer, unless treated and cured over three years ago; patients with cervical carcinoma in situ or non-melanoma skin carcinoma are eligible
- Inability to undergo regular monitoring due to geographical, social, or psychological reasons
- Patient under protective measures
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hôpitaux Civils de Colmar
Colmar, France, 68024
Actively Recruiting
Research Team
M
Massimo LODI, MD
CONTACT
M
Magali EYRIEY
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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