RecruitingNCT06761196
Quality of Life After Breast Cancer Surgery
Assessing Quality of Life After Breast Cancer Surgery: a Prospective Cohort Study
Sponsor
Centre Hospitalier de Colmar
Enrollment
1,500 participants
Start Date
Sep 2, 2025
Study Type
OBSERVATIONAL
Conditions
Summary
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.
Eligibility
Min Age: 18 Years
Inclusion Criteria6
- 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, whether for therapeutic or prophylactic purposes.
- Patient capable, in the opinion of the investigator, of complying with the requirements and restrictions of the study.
- Patient with a computer, tablet or smartphone connected to the Internet.
- Patient followed in the center on a regular basis according to standard recommendations.
Exclusion Criteria5
- Patient requiring surgical intervention under local anesthesia only.
- Patient requiring surgery for the installation or removal of an chemotherapy implantable port only.
- Patients with a history of cancer other than breast cancer. Patients with a history of cancer more than three years old are eligible if they are treated and considered cured. Patients with a history of cervical carcinoma in situ or non-melanoma skin carcinoma are eligible.
- Impossibility of being subject to regular monitoring for geographical, social or psychological reasons.
- Patient under protective measure
Interventions
OTHERQuestionnaire
The quality of life measured with different scales (BREAST-Q, EORTC QLQ C30 and BR42)
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06761196
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