Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Memory Gel and Shape Combined Cohort
NCT02919592 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to collect additional post-approval clinical data on the long-term performance of MemoryShape and MemoryGel Breast Implants, as indicated for primary or revisional breast augmentation and primary or revisional breast reconstruction.
Conditions Studied
Interventions
- DEVICE MemoryShape® Breast Implants
- DEVICE MemoryGel® Breast Implants
- PROCEDURE Other Aesthetic Surgery
Study Locations (20)
California
- Jaime Schwartz, MD — Beverly Hills
- Susan E. Downey, MD Inc — Burbank
- Mohebali Plastic Surgery — Corte Madera
- Institute of Cosmetic and Reconstructive Surgery — Fountain Valley
- Newport Beach Center for Plastic Surgery — Newport Beach
- Newport Center for Special Surgery — Newport Beach
- North Coast Plastic Surgery — Oceanside
- Li Plastic Surgery — Ontario
- Summit Plastic Surgery — Redding
- Verve Plastic Surgery — Solana Beach
- Kaweah Delta Health Care District — Visalia
Arizona
- Advanced Plastic Surgery Institute — Gilbert
- Advanced Surgical Associates — Mesa
- Robles Plastic Surgery — Phoenix
- Berardi Aesthetics and Plastic Surgery — Scottsdale
- Guerra Plastic Surgery Center — Scottsdale
- Mark Malek, MD Plastic Surgery — Scottsdale
Alabama
- Hedden Plastic Surgery Center — Birmingham
- Plastic Surgery of Tuscaloosa — Tuscaloosa
Arkansas
- Vanderpool Cosmetic Plastic Surgery — Fayetteville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 3,603 participants |
| Start Date | 2016-09-01 |
| Est. Completion | 2031-09-16 |
| Phase | NA |
Interested in This Trial?
Always speak with your doctor before enrolling in a clinical trial.
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02919592
The ClinicalTrials.gov registry entry for NCT02919592 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 3,603 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mentor Worldwide, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Primary Breast Augmentation appearing as the primary indexed condition, and to 3 interventions — of which MemoryShape® 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: NCT02919592 reports 20 study locations spanning 4 distinct geographic areas — top geographies include California, Arizona, Alabama. 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 NCT02919592 about?
NCT02919592 is a clinical study titled "Memory Gel and Shape Combined Cohort". The purpose of this study is to collect additional post-approval clinical data on the long-term performance of MemoryShape and MemoryGel Breast Implants, as indicated for primary or revisional breast augmentation and primary or revisional breast reconstruction.
What is the current status of trial NCT02919592?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 3,603 participants. The study started on 2016-09-01. Estimated completion is 2031-09-16.
What conditions does trial NCT02919592 study?
This clinical trial studies the following conditions: Primary Breast Augmentation, Primary Breast Reconstruction, Revision Breast Augmentation, Revision Breast Reconstruction. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02919592?
The interventions under investigation include: MemoryShape® Breast Implants (DEVICE), MemoryGel® Breast Implants (DEVICE), Other Aesthetic Surgery (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02919592?
This trial is sponsored by Mentor Worldwide, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02919592 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How Clinical Trials Work
Understand phases 1-4, trial design, randomization, and the informed consent process.
Patient Rights in Clinical Trials
Your rights as a participant: consent, withdrawal, privacy, and who to contact.
Finding the Right Clinical Trial
A practical guide to searching trials, understanding eligibility, and evaluating options.
All Guides
Browse our complete library of clinical trial educational resources.
Read our methodology — how this data is sourced, computed, and verified.