Motiva Implants® Post-Approval Study

NCT06938399 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2400

Last updated 2026-03-27

No results posted yet for this study

Summary

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.

Conditions

  • Breast Implant

Interventions

DEVICE

Silicone gel-filled breast implants - Motiva Implants®

Breast Surgery

OTHER

Aesthetic Surgery

Aesthetic procedure other than breast implant surgery

Sponsors & Collaborators

  • Motiva USA LLC

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
22 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-05-01
Primary Completion
2037-04-01
Completion
2037-07-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06938399 on ClinicalTrials.gov