About this trial
The investigators aim to document the surgery-specific and overall Quality of life parameters of patients undergoing all types of breast surgery at the University Hospital of Basel
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
adults who underwent any type of breast surgery at the University Hospital of Basel
Disqualifiers
Patients under the age of 18 years, without general consent or written informed consent, with insufficient language comprehension or other factors limiting their ability to co-operate in the study
Trial population
patients who underwent breast surgery at the University Hospital Basel from 2014 onwards
Trial design
Cohort
Other
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Patient satisfaction
five point likert-scale for satisfaction ( psychometric survey response scale ranging from "Strongly Disagree" to "Strongly Agree". The format includes: 1. Strongly Disagree, 2. Disagree, 3. Neutral (or Neither Agree nor Disagree), 4. Agree, and 5. Strongly Agree Descriptive measures using patient-reported outcome measures (BREAST-Q, McGill short form, EQ-5D-5L)
Patient reported quality of life
Descriptive measures using patient-reported outcome measures (BREAST-Q, McGill short form, EQ-5D-5L)
Sponsors and contacts
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