Quality of Life After Breast Cancer Surgery
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier de Colmar
About this trial
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 criteria
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Questionnaire
Treatment groups
No treatment groups listed
Sponsors and collaborators
Source ClinicalTrials.gov