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Quality of Life After Breast Cancer Surgery (SOCOM-QoL)

C

Centre Hospitalier de Colmar

Status

Enrolling

Conditions

Breast Cancer Surgery
Quality of Life

Treatments

Other: Questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT06761196
2024-A02572-45 (Other Identifier)
HCC-009

Details and patient eligibility

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.

Enrollment

1,500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Central trial contact

Magali EYRIEY; Massimo LODI, MD

Data sourced from clinicaltrials.gov

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