Study of the Safety and Effectiveness of Motiva Implants®
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT03579901 |
Recruitment Status :
Recruiting
First Posted : July 9, 2018
Last Update Posted : March 23, 2022
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Breast Implants | Device: Silicone gel-filled breast implants - Motiva Implants® Investigational breast implants | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 800 participants |
Allocation: | Non-Randomized |
Intervention Model: | Single Group Assignment |
Intervention Model Description: | Multicenter Single arm |
Masking: | None (Open Label) |
Primary Purpose: | Other |
Official Title: | Study of the Safety and Effectiveness of the Motiva Implants® Silicone Gel-Filled Breast Implants SmoothSilk® in Subjects Who Are Undergoing Primary Breast Augmentation, Primary Breast Reconstruction, and Revision Surgery |
Actual Study Start Date : | April 6, 2018 |
Estimated Primary Completion Date : | May 30, 2022 |
Estimated Study Completion Date : | August 30, 2033 |

Arm | Intervention/treatment |
---|---|
Primary Breast Augmentation
Subjects age 22 and over, indicated to increase breast size
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Device: Silicone gel-filled breast implants - Motiva Implants® Investigational breast implants
Breast augmentation |
Primary Breast Reconstruction
Subjects age 18 and over, Surgery to replace breast tissue that has been removed due to cancer, prophylactic mastectomy, breast trauma or that has failed to develop properly due to a severe breast anomaly.
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Device: Silicone gel-filled breast implants - Motiva Implants® Investigational breast implants
Breast augmentation |
Revision Augmentation
Revision surgery to correct or improve the results of a previous breast augmentation
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Device: Silicone gel-filled breast implants - Motiva Implants® Investigational breast implants
Breast augmentation |
Revision Reconstruction
Revision surgery to correct or improve the results of a previous breast reconstruction.
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Device: Silicone gel-filled breast implants - Motiva Implants® Investigational breast implants
Breast augmentation |
- Analyze and report the number of adverse events related to the use of the Silicone Gel filled Motiva Implants®. [ Time Frame: 10 Years ]Number of Participants with breast implants related adverse events as assessed by the incidence, severity, method of resolution and duration.

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years to 70 Years (Adult, Older Adult) |
Sexes Eligible for Study: | Female |
Gender Based Eligibility: | Yes |
Gender Eligibility Description: | Female |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria
- Genetic female.
- Patient is seeking one of the following procedures:
Primary Breast Augmentation Primary Breast Reconstruction Revision Augmentation Revision Reconstruction
- Patient has adequate tissue available to cover implant(s).
- Willingness to follow all study requirements including agreeing to attend all required follow-up visits and signs the informed consent.
- Agrees to have device returned to Establishment Labs if explanted.
- Willing to undergo Magnetic Resonance Imaging (MRI) evaluation of medically advised.
Exclusion Criteria:
- Has any breast disease considered to be pre-malignant in one or both breasts or is reporting mutations in BRCA1 or BRCA2 without a previous bilateral mastectomy or an untreated cancer of any type.
- Has inadequate or unsuitable tissue (e.g., due to radiation damage, ulceration compromised vascularity, history of compromised wound healing).
- Has an abscess or infection.
- Is pregnant or nursing or has had a full-term pregnancy or lactated within 6 months of enrollment.
- Is taking any drugs that would interfere with blood clotting, or that might result in elevated risk and or significant postoperative complications.
- Has any medical condition such as obesity (BMI ≥ 40), diabetes, autoimmune disease, chronic lung or severe cardiovascular disease that might result in unduly high surgical risk and or significant postoperative complications.
- Has any connective tissue/autoimmune disorder or rheumatoid disease, such as systemic lupus erythematosus, discoid lupus, scleroderma, or rheumatoid arthritis, among others.
- Has any condition that impedes the use of magnetic resonance imaging (MRI) including implanted metal device, claustrophobia or other conditions that would make MRI scan prohibited.
- Has a history of psychological characteristics that are unrealistic or unreasonable given the risks involved with the surgical procedure.
- Has been implanted with any non-FDA approved breast implant.
- Has been implanted with any silicone implant other than breast implants.
- HIV positive (based on medical history).
- Has been diagnosed with anaplastic large cell lymphoma (ALCL).
- Works for Establishment Labs, Motiva USA or any of their subsidiaries, the study surgeon, or ICON the Contract Research Organization (CRO) that is helping to conduct the study or are directly-related to anyone that works for Establishment Labs, Motiva USA or any of their subsidiaries, the study surgeon, or the CRO.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03579901
Contact: Laura Vindas, MD | +1 (833) 343-3263 | ustrial@establishmentlabs.com | |
Contact: Ana Vega, MD | +1 (833) 343-3263 | ustrial@establishmentlabs.com |

Responsible Party: | Motiva USA LLC |
ClinicalTrials.gov Identifier: | NCT03579901 |
Other Study ID Numbers: |
CLIN-17-008 |
First Posted: | July 9, 2018 Key Record Dates |
Last Update Posted: | March 23, 2022 |
Last Verified: | February 2022 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | Yes |
Device Product Not Approved or Cleared by U.S. FDA: | Yes |
Breast Implants Breast Surgery Breast Augmentation Breast Reconstruction |