Quality of Life After Breast Cancer Surgery
Recruiting · NCT06761196 · Observational (researchers observe without assigning treatment) · Lead sponsor: Centre Hospitalier de Colmar
View the official record on ClinicalTrials.gov →Interventions studied
Questionnaire
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.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- 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 criteria
- 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
Where it is running
1 location listed.
- Hôpitaux Civils de Colmar - Colmar, France