Summary

Eligibility
for females ages 18 years and up (full criteria)
Location
at San Francisco, California
Dates
study started
estimated completion
Principal Investigator
by Merisa Piper, MD

Description

Summary

The most common tissue expander-related infections are from Staphylococcus and Pseudomonas species. In addition, from breast tissue microbiome studies, Staphylococcus and Pseudomonas show variable abundance across samples. The investigator hypothesizes that breast cancer patients undergoing reconstructive surgery with high initial abundance of Staphylococcus and/or Pseudomonas are more likely to develop subsequent tissue expander-related infections from these respective organisms.

Official Title

Microbiome and Association With Implant Infections: Investigating the Impact of Antibiotics on the Gut and Breast Microbiomes Post-mastectomy With Implant-based Breast Reconstruction

Details

PRIMARY OBJECTIVE: a) To determine the feasibility of breast microbiome sampling using the study techniques SECONDARY OBJECTIVES: 1. To define the differences in the gut and breast microbiomes between patients undergoing mastectomy with implant-based reconstruction who develop post-operative implant infection and those who do not. 2. To determine the effects of post-operative antibiotics on the gut and breast microbiomes after mastectomy with implant-based reconstruction. Patients are followed-up for 90 days after undergoing implant-based reconstruction.

Keywords

Breast Cancer Breast Cancer Female Post-Surgical Antibiotics Breast Implant Infections Breast Microbiome Breast Reconstruction Mastectomy Infection Breast Neoplasms Cephalexin

Eligibility

You can join if…

Open to females ages 18 years and up

  1. Patients must have histologically confirmed breast malignancy
  2. Age >= 18 years
  3. Scheduled to undergo mastectomy with the immediate placement of tissue expanders
  4. Ability to understand a written informed consent document, and the willingness to sign it
  5. At least 4 weeks post-completion of chemotherapy

You CAN'T join if...

  1. Any significant medical condition or laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study
  2. Pregnant or breastfeeding
  3. Patients who have taken antibiotics within 90 days of the consent date
  4. Patients who have taken probiotics within 90 days of the consent date
  5. Patients who have a documented or reported allergic reaction to the outlined antibiotics to be used in this study
  6. Male patients

Location

  • University of California, San Francisco
    San Francisco California 94143 United States

Lead Scientist at UCSF

  • Merisa Piper, MD
    Assistant Professor, Surgery. Authored (or co-authored) 39 research publications.

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT05020574
Phase
Phase 2
Study Type
Interventional
Last Updated