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Motiva Implants® Post-Approval Study

RecruitingHealthy volunteers welcome

Motiva Implants® Post-Approval Study (PAS) Protocol for Motiva SmoothSilk® Round Ergonomix® ('Ergonomix®') and SmoothSilk® Round ('Round') Breast Implants in Subjects Who Are Undergoing Primary Breast Augmentation, Revision Augmentation and Other Aesthetic Procedures

Who can join

Ages 22 and older · Women · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria Motiva Implants®:

* Female
* Patient is seeking one of the following procedures: -Primary Breast Augmentation: age 22 and over, indicated to increase breast size -Revision Breast Augmentation: removal and replacement of breast implants (revision) to correct or improve the results of a previous breast augmentation
* Patient has adequate tissue available to cover implant(s)
* Willingness to follow all study requirements
* Signs an Informed Consent
* Agrees to have device returned to the Sponsor, if explanted
* Willing to undergo Computed Tomography Scan (CT), ultrasound, or MRI evaluation, if medically advised

Inclusion Criteria Control group:

* Is 22 years of age or older
* Female
* Is a candidate for aesthetic surgery (such as liposuction, rhinoplasty, face-lift)
* Signs an Informed Consent
* Willingness to follow all study requirements

Exclusion Criteria Motiva Implants®:

* Has any breast disease considered to be pre-malignant in one or both breasts or is reporting mutations in BRCA1 or BRCA2
* Has inadequate or unsuitable tissue (e.g., due to radiation damage, ulceration, compromised vascularity, history of compromised wound healing)
* Has an active infection anywhere in their body
* 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 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 Breast Implant Associated-Anaplastic Large Cell Lymphoma (BIA-ALCL)

Exclusion Criteria Control group:

* Has a history of silicone implants (anywhere in the body)
* Plans to undergo silicone breast implant surgery during the course of the study
* Has an active infection anywhere in their body
* Has a history of cancer (except skin cancer)
* 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

About the study

This study examines the general post-market use and safety of Motiva Implants® and gathers and assesses selected safety and effectiveness data about their post market performance and experience.

What is being tested

Sponsor: Motiva USA LLC · Participants: 2,400 · Started: May 1, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06938399

Locations in the U.S.

CaliforniaJ. Gerald Minniti, M.D., F.A.C.S., Beverly Hills
The Practice Healthcare, Beverly Hills
AESTHETX Center, Camp Pendleton
Los Gatos Plastic Surgery, Los Gatos
Align Surgical Associates Inc, San Francisco
Schwartz Aesthetic Institute, Westlake Village
ColoradoThe Center for Cosmetic Surgery, Denver
District of ColumbiaAdvanced Plastic Surgery, LLC, Washington D.C.
FloridaCareaga Plastic Surgery, Coral Gables
Alicia Billington Plastic Surgery LLC, St. Petersburg
IllinoisIteld Plastic Surgery, Chicago
Renee Burke Plastic Surgery, Aesthetics, & Med Spa, South Barrington
KentuckyCaloAesthetics® Plastic Surgery Center, Louisville
LouisianaThe Wall Center for Plastic Surgery, Shreveport
MarylandBelcara Health, Baltimore
Center for Plastic Surgery, Chevy Chase
MissouriParkcrest Plastic Surgery, St Louis
New JerseyDelaware Valley Plastic Surgery, Cherry Hill
Caroline A. Glicksman MD, Sea Girt
New YorkMark D. Epstein, MD, FACS Center for Aesthetic Surgery, Hauppauge
Neinstein Plastic Surgery, New York
North CarolinaCapizzi, MD Cosmetic Surgery & Med Spa, Charlotte
HKB Cosmetic Surgery, Charlotte
OklahomaJones Plastic Surgery, Oklahoma City
Landis Platic Surgery, Tulsa
TexasAustin Plastic Surgeon, Austin
Restora Austin Plastic Surgery Center, Austin
Dallas Day Surgery of Texas North, Dallas
Southwest Plastic Surgery, El Paso
Aesthetic Center for Plastic Surgery, Houston
Kristy Hamilton MD, FACS, Houston
North Texas Plastic Surgery, Southlake
UtahThe Plastics Clinic & SPA, South Jordan

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.