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NCT Number: NCT05736354

Molecular Mechanisms Associated With Breast Implant Complications

Bacterial biofilms cause implant failures, chronic inflammation, and immune polarization. The study investigates the possible role of bacterial biofilm as a factor in the etiology of Breast Implant Illness. Three patient cohorts will be studied (A) Subjects with breast implant with BII manifestations (B) Subjects with breast implants without BII manifestations (C) Subjects without breast implants who underwent breast surgery procedure. Blood, surgically discarded tissue, implants, and associated capsules will be collected through this protocol.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

IU Health North Hospital, Carmel, Indiana, United States

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About this study

Breast implants were first introduced in 1962. It is estimated that 10 million women worldwide, including three million Americans have breast implants. There has been increased identification of patients experiencing a constellation of symptoms related to their implants. For breast implants, these symptoms are often associated with autoimmune and connective tissue disorders (CTD) and have been referred to as Breast Implant Illness (BII). A growing number of patients 30,000 annually are seeking to have their breast implants removed. In view of the implant associated complications, the US Food and Drug Administration (FDA) has placed a black box warning on breast implants. Limited research has resulted in a void in the prognosis of this surgical problem. Bacterial biofilms are becoming a major concern for medical device implants. Bacterial biofilms cause implant failures, chronic inflammation, and immune polarization. The study investigates the possible role of bacterial biofilm as a factor in the etiology of BII.

This research studies oxilidized lipids (oxylipins). These are metabolities formed as a result of host-biofilm interaction. The presence of oxylipins will be studied in peri-prosthetic tissue post-biofilm infection and in systemic circulation. Oxylipins are immunogenic. Hence, the investigators will also study the abundance of immune cells T cells and macrophages (types and subtypes) and associated cytokines.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

for breast implant subjects:

  • Age greater than or equal to 18 years
  • Undergoing removal of breast implant
  • Willing and able to comply with protocol instructions

Inclusion criteria

for subjects undergoing breast surgeries (other than implant removal)

  • Age greater than or equal to 18 years
  • Undergoing breast surgery
  • Willing and able to comply with protocol instructions

Exclusion criteria

  • Individuals who are deemed unable to understand the procedures, risks, and benefits of the study, (i.e., unable to provide informed consent)
  • Pregnant females
  • Immunodeficiency (HIV/AIDS, SCID)
  • Currently on immunosuppressive medications
  • Prisoners

Treatment and study plan

Primary outcomes

  1. Presence of Biofilm in Breast Tissue

    Time frame: Through study completion, an average of 1 year

    During a clinically scheduled breast surgery, breast tissue specimens will be taken from surgically discarded tissue. The specimens from both breast implant subjects and control subjects (those undergoing breast surgery for a reason other than implant removal) will be analyzed to determine the presence of bacterial biofilm.

  2. Analysis of host-biofilm interaction mediated oxylipins from blood

    Time frame: Through study completion, an average of 1 year

    Prior to a clinically scheduled breast surgery, 20 milliliters of blood will be collected during the pre-operative surgical preparations. The blood samples from both breast implant subjects and control subjects (those undergoing breast surgery for a reason other than implant removal) will be analyzed for host-biofilm interaction mediated oxylipins.

  3. Cytokine analysis will be performed on breast tissue

    Time frame: Through study completion, an average of 1 year

    During a clinically scheduled breast surgery, breast tissue specimens will be taken from surgically discarded tissue. The specimens from both breast implant subjects and control subjects (those undergoing breast surgery for a reason other than implant removal) will undergo cytokine analysis.

  4. Analysis of host-biofilm interaction mediated oxylipins from breast tissue

    Time frame: Through study completion, an average of 1 year

    During a clinically scheduled breast surgery, breast tissue specimens will be taken from surgically discarded tissue. The specimens from both breast implant subjects and control subjects (those undergoing breast surgery for a reason other than implant removal) will undergo oxylipin analysis.

Secondary outcomes

  1. CD4+ Immunological Activation due to Host Implant Interaction

    Time frame: Through study completion, an average of 1 year

    Determining activation of CD4+ immune cells

Study contacts

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

Bryce Hockman

CONTACT

[email protected]

3172782715

Mithun Sinha, PhD.

CONTACT

[email protected]

3172782713

Sponsors and collaborators

Lead sponsor

Indiana University

Other

Collaborators

  • National Institute of Allergy and Infectious Diseases (NIAID)
  • National Institutes of Health (NIH)

Registry information

Acronym: MMABIC

Important dates

Study start
2021
Primary completion
2028
Study completion
2028
First posted
Feb 21, 2023
Registry last updated
Jun 11, 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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