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ACTIVE NOT RECRUITING NA

Study of the Safety and Effectiveness of Motiva Implants®

NCT03579901 · View on ClinicalTrials.gov ↗

Study Summary

This study evaluates the safety and effectiveness Motiva Implants® in women who are undergoing primary breast augmentation, primary breast reconstruction or revision breast surgery.

Conditions Studied

Interventions

  • DEVICE Silicone gel-filled breast implants - Motiva Implants® Investigational breast implants

Study Locations (20)

New York

  • Mark D. Epstein, MD, FACS/ Center for Aesthetic Surgery — Hauppauge
  • NYU Plastic Surgery Associates — New York
  • May Center for Mount Sinai Doctors — New York
  • Fifth Avenue Millennium Aesthetic Surgery, PLLC — New York

California

  • Gerald Minitti, MD, FACS — Beverly Hills
  • Steven Teitelbaum, MD, FACS — Santa Monica
  • Westlake Cosmetic Surgery Center — Westlake Village

Illinois

  • Northwestern Plastic Surgery — Chicago
  • Northwestern Specialists in Plastic Surgery, S.C. — Chicago

Oregon

  • Movassaghi Plastic Surgery & Ziba Medical Spa — Eugene
  • Portland Plastic Surgery — Portland

Colorado

  • The Center for Cosmetic Surgery — Golden

Georgia

  • Emory University Hospital — Atlanta

Indiana

  • Meridian Plastic Surgery Center — Indianapolis

Kentucky

  • CaloAesthetics® Plastic Surgery Center — Louisville

Trial Details

FieldValue
Enrollment Target 800 participants
Start Date 2018-04-06
Est. Completion 2033-02-28
Phase NA

Sponsor

Motiva USA

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03579901

The ClinicalTrials.gov registry entry for NCT03579901 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 800 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Motiva USA, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Breast Implants appearing as the primary indexed condition, and to 1 intervention — of which Silicone gel-filled breast implants - Motiva Implants® Investigational breast implants is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03579901 reports 20 study locations spanning 13 distinct geographic areas — top geographies include New York, California, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03579901 about?

NCT03579901 is a clinical study titled "Study of the Safety and Effectiveness of Motiva Implants®". This study evaluates the safety and effectiveness Motiva Implants® in women who are undergoing primary breast augmentation, primary breast reconstruction or revision breast surgery.

What is the current status of trial NCT03579901?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 800 participants. The study started on 2018-04-06. Estimated completion is 2033-02-28.

What conditions does trial NCT03579901 study?

This clinical trial studies the following conditions: Breast Implants. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03579901?

The interventions under investigation include: Silicone gel-filled breast implants - Motiva Implants® Investigational breast implants (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03579901?

This trial is sponsored by Motiva USA, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03579901 being conducted?

This trial has 20 study locations across California, Colorado, Georgia, Illinois, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial