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Study identifier: NCT07059104 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Implant-based Breast Reconstruction in Post-bariatric Women - a Registry-based National Study

Condition: Breast Cancer · Breast Reconstruction · Bariatric Surgery  ·  Sponsor: Vastra Gotaland Region

PhaseN/A
Planned participants20000
Who can joinFemale, N/A to no upper limit
Healthy volunteersNo

About this study

The goal of this national registry-based study is to investigate the prevalence of reconstructive breast surgery and risk factors for surgical complications in women who have had weight loss surgery previously. The main questions it aims to answer are: 1. What is the perceived need for breast implants after weight loss surgery, described as the proportion who have breast implants, and what characteristics, in terms of demographics and surgical details, do the operated women have? 2. In women who have breast enlargement or breast enlargement combined with a lift, are there any differences between the women who have had weight loss surgery and other women regarding complications after the operation and characteristics of the surgery, for example skin incision and choice of implant (for example texture, shape, size)? 3. In women who have delayed breast reconstruction after breast cancer, that is have had their breast/s reconstructed in a separate operation, are there any differences between the women who have had weight loss surgery and other women regarding complications after the operation and characteristics of the surgery, for example in technique used (autologous versus implant-based, choice of implant, such as texture, shape and size), and timing of the surgery? Immediate breast reconstruction is defined as performed at the same time as the mastectomy, and delayed as an operation performed later in a separate operation. 4. In women who have immediate breast reconstruction…

This description comes directly from the study's public registry record.

Talk to the study team

Emma Hansson, Professor, MD, Phd, MA  ·  +46313421000  ·  emma.em.hansson@vgregion.se

Always discuss trial participation with your own doctor first.

Locations (1)

Västra GötalandsregionenGothenburg, SwedenRecruiting

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Source record: clinicaltrials.gov/study/NCT07059104