Biopsy-site Marker Effects in Breast Cancer

Biopsy-site-marker in Breast Cancer

Recruiting Observational Study
Breast Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Female
Study type
Observational
Participants needed
140 (estimated)
Sponsor
University of Oklahoma · Other
Who this trial is looking for

This trial is looking for women over 18 who have been diagnosed with invasive breast cancer. Participants will help researchers understand how the stiffness of a biopsy site marker might affect inflammation in breast cancer.

Are You a Good Fit for This Trial?
Rules you out Severe uncontrolled systemic diseasesActive viral infections

You may be able to join if

  • I have signed a consent form to participate.
  • I am a female over 18 years old.
  • I have been diagnosed with invasive breast cancer.

You may not be able to join if

  • I have had a biopsy at OUBI OKC.
  • I am going to receive neoadjuvant therapy.
  • I have uncontrolled high blood pressure or diabetes.
  • I am currently pregnant or breastfeeding.
  • I am not eligible for surgery.
  • I am a prisoner.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

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About This Trial

The purpose of this study is to explore pro-metastatic changes in breast cancer (BC) associated with the stiffness of biopsy site markers. This study aims to determine whether the stiffness of a biopsy site marker promotes inflammatory changes in breast cancer and to evaluate whether there is a relationship between biopsy site marker stiffness and inflammation.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Written informed consent (ICF) signed and dated by the patient prior to the performance of any study-specific procedures, sampling, or analyses. * Female patients at \> 18 years of age at the time of signature of the ICF. * Pathologically verified invasive breast cancer cases …
Contacts

Lead Onco Nurse

405-271-8777

SCC-IIT-Office@ouhsc.edu

CONTACT

Takemi Tanaka, PhD

takemi-tanaka@ou.edu

CONTACT