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| Protocol Number: |
No date |
| Trial Phase: |
Phase I |
| IRB Number: |
UL IRB # 094.02JH |
| Study Status: |
Active |
| Enrollment Status: |
Open |
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| The purpose of this study is to collect safety data associated with the implantation of its gel-filled mammary prosthesis. |
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Eligibility |
Inclusion Criteria: 1. Must be female (genotypical females only), AND
2. The patient must be willing to follow the study requirements to include:
a. Sign the Informed Consent Document before surgery is performed.
b. Agree to complete all required follow-up visits.
c. For those patients who wish to participate in the Patient Registry: agree to conditions of the Implant Regitry and follow the requirements of the Registry program.
d. Agree to follow Mentor Standard Operating Procedures for explant analysis in which case the patient may be asked to authorize the sponsor to complete analysis on any study device (s) which may require removal throughout duration of the study.
e. Must be determined by the investigator and other medical specialists (as required) to be an acceptable candidate for reconstructive breast surgery. General medical condition and history, as well as psychological appropriateness should be considered before surgical intervention, AND
3. In the medical opinion of the surgeons conditions must be such that saline implants are deemed unsuitable for the patient. (Patient procedures for gel implants is NOT considered a medical condition.) Examples of saline unsuitability are:
a. Severe wrinkling of an existing saline implant to the extent that it would be considered a severe deformity (implant must have been in place longer than 6 months).
b. Unilateral replacement (opposite breast is gel).
c. Tissue or skin is too thin to support a saline implant.
d. Previously dissected pocket is incompatible with saline implant (profile), AND
4. The patient must have one or more of the following breast conditions:
a. Post-unilateral or bilateral mastectomy (immediate or delayed) as a result of cancer or other disease process.
b. Require reconstruction due to cancer treatments other than mastectomy.
c. Require a revision due to complications or other undesirable results of a previous surgery for the above reasons.
d. Post-Trauma defined as total or partial removal of the breast(s) through surgery (for any reason) or as a result of the trauma itself.
e. Congenital deformities defined as:
- Pectus Excavatum defined as congenital concave chest wall deformity with abnormalities of the sternum and anterior ribs.
- Pectus Carinatum defined as convex chest wall deformity with abnormalities of the sternum and anterior ribs.
- Severe asymmetry defined as congenital or acquired substantial discrepancy in breast sizes such as to represent a significant physical deformity or abnormality ( e.g. Poland's syndrome).
f. Severe ptosis defined as requiring a reconstruction procedure such as a mastopexy (tissue and/or skin must be removed from the breast to qualify as a mastopexy procedure).
g. Patients who require revision with implant replacement for severe deformity caused by medical or surgical complications, regardless of original indiction for implantation or type of device originally implanted.
h. Replacement or revision for patients whose prior surgery was not a result of treatment for cancer and for whom saline implants are unsuitable (e.g. skin too thin, insufficient tissue, etc) as deemed by the surgeon.
- Size changes (larger or smaller) are only allowed if the investigator determines that a revision or replacement is required for medical reasons. In a case where a change of size is the only indication for surgery, and no medical necessity exists, the protocol will not allow replacement.
j. Patients who require Augmentation mammaplasty in the unaffected breast as a result of the surgery, due to one of the above indications, in the affected breast (i.e., unilateral mastectomy with augmentation to opposite breast to provide symmetry).
j. Special circumstances for implantation will be considered on a case by case basis per written FDA authorization. |
Exclusion Criteria: 1. Augmentation mammaplasty and the failure to have at least one of the diagnoses identified in the inclusion criteria.
2. Have an abscess or infection anywhere in their body at the time of study entry.
3. Be currently pregnant or nursing.
4. Be diagnosed as having lupus defined as Systemic Lupus Erythematosus or Discoid Lupus, or scleroderma defined as Progressive Systemic Sclerosis.
5. Currently have uncontrolled diabetes or any diseases which are clinically known to impact wound healing ability.
6. Demonstrate tissue characteristics which are clinically incompatible with mammaplasty ( e.g. tissue damage resulting from radiation, inadequate tissue, compromised vascularity or ulceration).
7. Possess any condition or currently be under treatment for any condition, which in the opinion of the investigator and/or consulting physician (s), may constitute an unwarranted surgical risk.
8. Demonstrate psychological characteristics such as inappropriate attitude or motivation which, in the opinion of the investigator are incompatible with the risks involved with the surgical procedure and prosthesis.
9. Unwillingness to undergo any further surgery for revision (if required). |
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