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Not yet recruiting NCT07699913

Quality of Life of Patients Who Have Undergone Bilateral Mastectomy

— Observational Surgery Date Age BMI Height

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Surgery Date, Age, BMI, Height. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Psychological Experience, Quality of Life, and Patient Satisfaction Following Bilateral Breast Reconstruction After Prophylactic or Therapeutic Mastectomy, Using the BREAST-Q Questionnaire.

Overview

The investigators therefore aim to determine whether the type of mastectomy (preventive in a high-risk patient or therapeutic in a patient with a history of cancer), as well as the timing (immediate or delayed) and type of breast reconstruction, influence the quality of life and satisfaction of patients who have undergone bilateral mastectomy. The goal of this observational study is thus to measure and compare the quality of life of patients who have undergone bilateral mastectomy using the BREAST-Q questionnaire.

Primary outcome measures

  • Measure of the BREAST Q Questionnaire [Time frame: 3 months post operatively]

Eligibility criteria

Inclusion criteria

  • Female sex
  • Age ≥ 18 years
  • Bilateral mastectomy
  • Breast reconstruction between January 1, 2015, and January 1, 2026
  • No objection to the study

Exclusion criteria

  • Individual under guardianship or curatorship, or deprived of liberty
  • Reconstruction not completed by January 1, 2026.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07699913 · 2026-A00794-47

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗