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Patient Reported Outcomes After Oncoplastic Breast Conserving Surgery

NCT05724758 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2023-02-13

No results posted yet for this study

Summary

The goal of this study is to assess patient satisfaction after oncoplastic breast conserving surgery. With the help of a breast-questionnaire the patient satisfaction will be assessed before the surgery and 4 weeks, 6 months and 1 year after the operation. The main question it aims to answer are: Does breast conserving surgery improve quality of life.

type of study: cohort study, observational

OCBS = oncoplastic breast conserving surgery BCT = breast conserving therapy DCIS = ductal carcinoma in situ

participant population/health conditions

* Patients with newly diagnosed breast cancer, that can be treated breast conserving
* the participants have to be at least 18 years old

Participants will fill out a questionnaire pre surgery, 4 weeks, 6 months and 1 year after the surgery. The individual questionnaires will be compared.

Conditions

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

Interventions

PROCEDURE

Breast-conserving surgery

Following oncoplastic surgeries are performed at the Brust-Zentrum in Zurich: * Oncoplastic reconstruction with round-block technique * Oncoplastic reconstruction using J-Plastic * Oncoplastic reconstruction using V-Plastic * Oncoplastic reconstruction using Grisotti * Oncoplastic reconstruction using Batwing * Oncoplastic reconstruction using Mammareductionplasty (Wise Pattern, Vertical) * Oncoplastic perforator flap surgery

Sponsors & Collaborators

  • Brust-Zentrum AG

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-01
Primary Completion
2023-09-01
Completion
2024-09-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05724758 on ClinicalTrials.gov