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Enrolling by invitation NCT07623564

Clinical Study on Tissue Preservation in Breast Augmentation and Reconstruction

— Observational Breast Augmentation and Breast Reconstruction Mammaplasty Breast Augmentation Tissue Preservation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Mia Harmonization, Mia Scarless Lift, Mia Reconstruction, Joy Dot.
Who it may be relevant to
Registry conditions: Breast Augmentation and Breast Reconstruction, Mammaplasty, Breast Augmentation, Tissue Preservation. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Costa Rica
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Post-Marketing Clinical Follow-Up Study on Tissue Preservation Techniques in Breast Augmentation and Reconstruction.

Overview

This clinical study aims to evaluate the safety and effectiveness of advanced, minimally invasive techniques for breast augmentation and reconstruction. These methods, known as Mia Harmonization, Mia Scarless Lift, Mia Reconstruction, Joy Dot, and Maxtopexia + Mia, focus on preserving breast tissue, reducing recovery time, and improving aesthetic outcomes.

Detailed description

This post-marketing observational study evaluates the safety and efficacy of innovative, minimally invasive breast augmentation and reconstruction techniques: Mia Harmonization, Mia Scarless Lift, Mia Reconstruction, Joy Dot, and Maxtopexia + Mia. These techniques aim to enhance tissue preservation, minimize scarring, and promote quicker recovery compared to traditional methods.

The study will enroll 60 participants undergoing these procedures at the Sulàyöm Innovation Campus in Costa Rica between January and December 2025. Participants will be followed for 36 months to monitor complication rates, tissue health, and satisfaction. Procedures utilize advanced devices like the Motiva Ergonomix2® Diamond®, Motiva Injector®, Motiva® Inflatable Balloon, and Motiva® Reusable Channel Separator, designed to optimize outcomes while preserving natural breast structures.

Key assessments include:

Safety Metrics: Monitoring adverse events, such as tissue necrosis, hematoma, or infection, through regular follow-ups.

Efficacy Metrics: Evaluating tissue preservation during and after surgery using imaging and clinical assessments.

Patient and Surgeon Satisfaction: Measuring perceptions of outcomes and procedure success using validated scales.

The study will also conduct a temperature monitoring substudy using the Motiva® Zen transponder to assess its functionality in recording implant temperature. This optional component enhances understanding of implant safety.

Results will provide crucial insights into the role of minimally invasive techniques in improving breast surgery outcomes, focusing on safety, tissue preservation, and patient satisfaction. These findings will inform future surgical practices and technological advancements.

Interventions

  • Procedure Mia Harmonization
    Minimally invasive technique for breast augmentation, increasing volume while preserving natural tissue.
  • Procedure Mia Scarless Lift
    Minimally invasive breast lift for mild to moderate ptosis without visible scarring.
  • Procedure Mia Reconstruction
    Reconstructive technique for restoring breast contour and volume after benign surgical interventions.
  • Procedure Joy Dot
    Advanced augmentation method using specialized tools to preserve tissue integrity and minimize trauma.
  • Procedure Maxtopexia + Mia
    Breast lift combining traditional techniques with advanced minimally invasive methods for tissue preservation.

Primary outcome measures

  • Number of Adverse Events Related to Tissue Preservation [Time frame: 36 months post-surgery.]
  • Rate of Intraoperative Tissue Integrity Preservation [Time frame: Day of surgery.]
Secondary outcome measures (3)
  • Patient-Reported Satisfaction Score (5-Point Likert Scale) [Time frame: Baseline and follow-ups at 1, 3, 6, 12, 24, and 36 months post-surgery.]
  • Surgeon-Reported Satisfaction Score (5-Point Likert Scale) [Time frame: Day of surgery.]
  • Rate of Postoperative Complications [Time frame: 36 months post-surgery.]

Eligibility criteria

Inclusion criteria

  • Gender and Age: Cisgender women, aged 18 years or older.
  • Surgical Procedure: Participants undergoing primary breast augmentation or benign reconstruction using the following minimally invasive procedures:
  • Mia Harmonization
  • Mia Scarless Lift
  • Mia Reconstruction
  • Joy Dot
  • Maxtopexia + Mia
  • Breast Size: Cup sizes AA to C, as determined by guidelines from Triumph International.
  • Health Status: ASA (American Society of Anesthesiologists) classification I or II.
  • Tissue Integrity: Adequate breast tissue available to cover the implant(s).
  • Commitment: Willingness to adhere to all study requirements, including follow-up visits and signing the informed consent form.
  • Special Cases for Reconstruction: Participants with congenital or acquired breast or thoracic conditions, such as amastia, pectus excavatum/carinatum, tuberous breasts, or asymmetry.
  • Mia Scarless Lift Specifics: Participants with mild, moderate, or pseudoptosis based on physician evaluation.
  • Timing: Women scheduled for surgery at the Sulàyöm Innovation Campus between January and December 2025.

Exclusion criteria

  • Non-Specified Procedures: Women undergoing augmentation or reconstruction with techniques other than those listed (Mia Harmonization, Mia Scarless Lift, Mia Reconstruction, Joy Dot, Maxtopexia + Mia).
  • Non-Study Implants: Use of implants other than Motiva products.
  • Compromised Tissue or Skin:
  • Existing rib lesions or significant/severe breast ptosis.
  • Poor tissue quality due to radiation damage, vascular compromise, or prior ulceration.
  • Medical History:
  • History of breast abscesses or infections.
  • Sensitivity or allergy to silicone.
  • Current Physiological Conditions:

-Pregnancy or breastfeeding, or within six months postpartum or post-lactation.

  • Medications: Use of anticoagulants or medications that impair wound healing (e.g., corticosteroids, Warfarin).
  • Imaging Constraints: Conditions that prevent the use of MRI (e.g., implanted metal devices, claustrophobia).
  • Concurrent Research: Participation in another clinical research study involving drugs or devices.
  • Follow-Up Barriers: Residency outside Costa Rica or inability to attend required follow-up visits.
  • Timing Issues: Participants undergoing surgery outside the designated study period (January to December 2025).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Costa Rica · 1 center
  • Establishment Labs — Coyol

Identifiers

NCT: NCT07623564 · CIP-001003

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗