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NCT Number: NCT07810257

Prospective Longitudinal Cohort Study of Implant Age, Pocket Plane, Incision, Surface Texture, and Volume as Predictors of Breast Implant Shell Fissure

This prospective implant-surveillance cohort will evaluate predictors of breast implant shell fissure. Women with aesthetic implants without baseline fissure or rupture will undergo annual clinical and imaging assessment for up to five years. Implant age, pocket plane, incision route, surface texture, and volume will be evaluated as predictors. The primary outcome is time to first confirmed focal shell fissure; progression to complete rupture, symptoms, inter-reader agreement, and revision will also be assessed.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

A locked radiologic and operative definition will distinguish focal shell fissure from complete rupture, deformation, porosity, and leakage. Eligible women will enter only after baseline imaging shows no shell defect. Annual ultrasound and confirmatory MRI will prospectively identify incident events, which will undergo central blinded review and surgical confirmation when available. Delayed-entry time-to-event models will evaluate implant and surgical predictors and will account for bilateral implants and competing removal. A multi-state analysis will explore progression from intact implant to fissure and rupture if the event count is adequate.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female sex and age 18 years or older.
  • Aesthetic breast implant with known implantation date or year and known pocket plane, incision route, surface texture, and volume.
  • No fissure or rupture identified by the baseline imaging algorithm.
  • Ability to undergo annual ultrasound and confirmatory MRI when indicated.
  • Written informed consent.

Exclusion criteria

  • Confirmed fissure or rupture at cohort entry.
  • Reconstructive breast implantation or tissue expander.
  • Immediate planned implant removal or exchange.
  • Missing core implant characteristics.
  • MRI contraindication when MRI is required to adjudicate a suspected event.
  • Recalled/PIP implant if excluded by the final analytic plan.

Treatment and study plan

Breast Implant Exposure

Device

Recorded characteristics include implant age, material, surface texture, shape, volume, pocket plane, incision route, manufacturer/lot when available, primary or revision placement, and laterality. Linked arm/group(s): Implant Shell Integrity Surveillance Cohort.

Structured Implant Shell Imaging

Diagnostic Test

Annual high-resolution ultrasound and confirmatory MRI will apply a locked definition of focal shell fissure, complete rupture, deformation, porosity, and silicone leakage. Event images will undergo blinded central review. Linked arm/group(s): Implant Shell Integrity Surveillance Cohort.

Primary outcomes

  1. Time to First Confirmed Breast Implant Shell Fissure

    Time frame: From cohort entry through years of prospective follow-up. 10 years

    Implant-level time from cohort entry to the first focal partial-thickness or noncomplete shell discontinuity meeting the locked MRI, ultrasound, or operative criteria and not meeting the definition of complete rupture.

Secondary outcomes

  1. Fissure-Free Survival by Implant Age

    Time frame: 10 years

    Probability of remaining free of confirmed fissure at prespecified implant ages using delayed-entry survival methods.

Study contacts

Contact information is provided by the study sponsor or research team.

Juan Velez, MD, Plastic surgeon

CONTACT

[email protected]

+57 3054511588

Sponsors and collaborators

Lead sponsor

Research Inc

Industry

Registry information

Important dates

Study start
2014
Primary completion
2026
Study completion
2026
First posted
Sep 9, 2026
Registry last updated
Sep 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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