The Impact of Breast Surgery on Patients' Quality of Life

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-05-16

Study Completion Date

2035-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Aspects of Breast-conserving Surgery

NCT04227613

Breast Neoplasm Cosmetic Outcome Quality of Life

COMPLETED

Quality of Life After Conservative Oncoplastic Surgery in Breast Cancer Patients (IRONY: lIfe afteR ONcoplastic surgerY)

NCT05842148

Breast Cancer

RECRUITING

Quality of Life After Breast Cancer Surgery

NCT06761196

Breast Cancer Surgery Quality of Life

RECRUITING

Emotional Security and Quality of Life Among Breast Cancer Patient Who Have Undergo Mastectomy

NCT04872803

Mastectomy

UNKNOWN

Patient Reported Outcomes After Oncoplastic Breast Conserving Surgery

NCT05724758

Breast Cancer Stage I Breast Cancer Stage II Breast Cancer in Situ

UNKNOWN

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The planned ten-year follow-up using Patient reported outcome measure will give us the unique opportunity to gain insight into patients' breast-related QoL (Quality of Life) long after surgery and detect systematic issues that may affect them beyond the scope of routine follow-up consultations. Along with the detection of any occurring adverse events, the information gathered in the database will facilitate the search for risk factors involved in their development, ideally resulting in their rectification and thus contributing to patient well-being in the long term.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Breast Surgery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* adults who underwent any type of breast surgery at the University Hospital of Basel

Exclusion Criteria

* 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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No