Breast Reconstruction Surgery

3

Review clinical trials related to Breast Reconstruction Surgery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Post-market Prospective Clinical Study of Nagor Perle Mammary Implants

Patients can undergo breast implant surgery for multiple reasons; cosmetic and reconstructive being the primary indications. In order to confidently state safety and due to strict regulation on medical devices it is important to maintain a record of safety and performance with all medical implants. This study is designed to collect data on a new generation of smooth mammary implants to assess the long term performance and safety data on this type of gel-filled mammary breast implant. The two main complications of breast implants are capsular contracture and rupture; these complications can take years to develop. The study is designed to evaluate the occurrence of these two primary complication as well as other secondary complications over a period of 10 years. Patient follow up will be carried out pre-operatively and post operatively at 12 months and then 3, 5, 8 and 10 years thereafter. The study will be carried out over 10 years to adequately assess complications which may only occur over the lifetime of the device such as systemic complications

Participants needed: 60
Trial details
Age: 18-65Biological sex: FemaleType: ObservationalSponsor: GCA (Eurosilicone)Updated: Jun 29, 2026Locations: 1
Eligibility criteria

Genetic female subjects aged ≥18 and ≤65 [+1]

Subjects undergoing implant augmentation with a BMI > 30 and undergoing reconstr... [+12]

Status: Recruiting

Tissue Reinforcement for Breast Reconstruction (TRBR) Pivotal Clinical Study (REDEFINE)

The GORE Tissue Reinforcement for Breast Reconstruction (TRBR) research study will look at breast reconstruction during mastectomy procedures. There will be two arms in this study, a Treatment Arm, where data will be collected for a new medical device called the Tissue Reinforcement for Breast Reconstruction (TRBR) Device and a Control Arm where data will be collected from subjects who have previously had surgery and received no additional tissue reinforcement in their breast reconstruction surgery. This research study will look at the safety of the Study Device and the success of the participants breast reconstruction. The Study Device is investigational, which means it has not yet been used nor approved by the FDA for this treatment. The data collected in this study will be compared to the data collected in the Control Arm.

Participants needed: 180
Trial details
Age: 22+Biological sex: FemaleType: InterventionalSponsor: W.L.Gore & AssociatesUpdated: Oct 23, 2025Locations: 20
Eligibility criteria

Female subjects ≥ 22 years of age. [+5]

Subject has had a revision(s) in the target breast(s) following complications of... [+14]

Status: Recruiting

PARTial BREast RECONstruction With Chest Wall Perforator Flap

The goal of this observational study is to ascertain the outcomes following partial breast reconstruction using chest wall perforator flaps after breast conservation surgery.

Participants needed: 1,001
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Cambridge University Hospitals NHS Foundation TrustUpdated: Dec 11, 2024Locations: 1Duration: 6 Months
Eligibility criteria

Patients undergoing partial breast reconstruction using CWPF for primary breast... [+3]

Patients undergoing volume displacement BCS [+1]