PERLE10PMCF: Post-market Prospective Clinical Study of Nagor Perle Mammary Implants
Study Details
Study Description
Brief Summary
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
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Smooth Silicone Breast Implant
|
Device: PERLE Sterile Smooth Opaque gel filled mammary implants
Sterile smooth opaque gel filled mammary implants will be implanted in adult women having breast surgery for either augmentation, reconstruction or revision surgery. Different ranges of implants will be used to suit patient needs
|
Outcome Measures
Primary Outcome Measures
- Rate of capsular contracture (Baker grade III-IV) [10 years post-surgery]
- Rate of implant rupture [10 years post-surgery]
Secondary Outcome Measures
- Rate of the secondary surgical procedures required for correction of complications [10 years post-surgery]
- Rate and frequency of local complications associated with the use of Nagor gel-filled mammary implants [10 years post-surgery]
Capsular contracture of Baker Grade I-II Haematoma Rupture Seroma Severe and continuing pain Post-operative infection Explantation as a result of infection Implant displacement/extrusion Wrinkling/folds Breast Implant Associate Anaplastic Large Cell Lymphoma BII/Asia Delayed or abnormal wound healing occurring within the first 3 months of surgery Any other complications considered by the Investigator to be related to the device or surgical procedure
- Patient satisfaction [10 years post-surgery]
BREAST- Q method
- rate and frequency of any adverse events [10 years post-surgery]
Eligibility Criteria
Criteria
Inclusion Criteria:
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Genetic female subjects aged ≥18 and ≤65
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Subjects who underwent single or bilateral breast implantation with the study device for one of the following reasons:-
- Primary breast reconstruction following mastectomy (both for one-stage or two-stage surgeries, including patients with previous radiotherapy and who have ADMs of animal origin (bovine, porcine)). ii) Primary breast augmentation (cosmetic surgery) with or without mastopexy iii) Breast revision surgery with or without mastopexy c) Subjects who have received a Nagor PERLE implant. d) Subjects who have provided informed consent and can adhere to the requirements of follow up appointments as per the study protocol.
Exclusion Criteria:
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Subjects undergoing implant augmentation with a BMI > 30 and undergoing reconstruction with a BMI >32.
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Subjects with autoimmune disease, lung fibrocystic disease, conditions that interfere with wound healing and blood clotting, a weakened immune system, reduced blood supply to the breast tissue or any other condition for which breast implants are contraindicated.
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Subjects who have participated in a clinical study which involve chemical or drug study within 3 months prior to surgery, with the exception of subjects who are participating in breast cancer related clinical studies.
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Subjects with insufficient tissue covering due to either radiation damage on the chest wall, tight thoracic skin grafts or radical resection of the pectoralis major muscle.
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Subjects who have ADMs of synthetic origin.
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Subjects who, in the Investigator's clinical opinion, have existing local or metastatic carcinoma of the breast that is unlikely to be fully excised at the time of insertion of the breast implant.
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Subjects with known previous history of a sensitivity to silicone who, in the opinion of the Investigator, are unsuitable for surgery.
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Subjects with an active infection who are unsuitable for surgery unless, in the opinion of the investigator, they are treated and cleared by the investigator.
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Subjects with a history of abscesses anywhere in the body who, in the opinion of the Investigator, are unsuitable for surgery.
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Subjects with a known history of compromised wound healing.
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Subjects who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up in this study.
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Women who are pregnant and/or current breast feeders who do not stop breast feeding within 3 months of getting breast implants
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Patients who have local recurrence or metastatic carcinoma at the time of insertion of breast implant
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- GC Aesthetics
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- DM6 640 0101