Abilene, TXNCT06643767Now EnrollingIRB Ready

Breast Cancer Clinical Trial in Abilene, TX

Access cutting-edge breast cancer treatment through this clinical trial at a research site in Abilene. Study-provided care at no cost to qualified participants.

Sponsored by Sure, Inc.

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Expert Care in Abilene

Access breast cancer specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related breast cancer treatment provided free

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Check if you qualify for this breast cancer clinical trial in Abilene, TX

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Abilene

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Abilene site if eligible
  4. 4Begin participation

About This Breast Cancer Study in Abilene

Objective: The "Bexa Breast Exam," or "BBE," for the purposes of this study is defined as the use of a Bexa device in conjunction with a portable, focused ultrasound examination to identify and further evaluate abnormal breast masses including cancer. Commercially, this combination of Bexa plus focused ultrasound is called "Bexa Breast ExamTM," and abbreviated as, "BBE." This study compares the Bexa Breast Exam (BBE) to the standard of care (digital breast tomosynthesis) in detecting masses and as a breast cancer early detection examination. The specific objectives are: 1. To measure the sensitivity and specificity of BBE as compared to digital breast tomosynthesis in the general population of women over 30 without a history of breast cancer. 2. To measure the sensitivity and specificity of BBE as compared to digital breast tomosynthesis identifying breast masses including cancer in women with dense breasts. 3. To demonstrate the proportion of women receiving a BBE that require additional imaging studies. Hypothesis: The purpose of this study is to demonstrate that the Bexa Breast Examination's sensitivity and specificity in identifying abnormal breast masses is comparable to the current accepted standard of care, mammography with tomosynthesis.

Sponsor: Sure, Inc.

Who Can Participate

Inclusion Criteria

Women who present to receive a screening mammogram.
Women of all races, ethnicities, and socio-economic backgrounds.
Signed informed consent obtained prior to any study assessments and procedures.
Age 30-75 years of age and female.

Exclusion Criteria

Women with findings that are \< 0.5 cm or \> 3.5 cm
Palpable lesion (to the participant)
Positive clinical findings that cause a visible and obvious deformity of the breast or alteration in the skin appearance of the breast.
Women with breast tenderness significant enough to prevent completion of any of the study examinations. (Both ultrasound and Bexa require a light degree of pressure on the breast; certain women, very few, have enough breast tenderness that they cannot tolerate the pressure of either Bexa or ultrasound. Mammograms exert substantially more pressure on the breast.)
Women with breast significant skin scarring enough to prevent effective BBE (e.g., keloid scarring of the breast, for example), because extensive, hard surface scarring introduces artifact in the Bexa exam. Participant exclusion will be determined by the Bexa examiner.
Greater than 3 positive findings in a given breast.
Women who are unable to comprehend or unwilling to sign an informed consent form.
Women ages \< 30 and \> 75 years of age.
Pregnant women.
Women who have had a mastectomy - unilateral or bilateral.
Women who have had a recent (past 30 days) biopsy performed.
Women who have had a prior history of breast cancer in either breast.
Women who have had radiation to the breast.
Women who have had any breast surgery within the last 12 months.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Abilene?

Yes, this clinical trial (NCT06643767) has an active research site in Abilene, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Breast Cancer Treatment Options in Abilene, TX

If you're searching for breast cancer treatment options in Abilene, TX, this clinical trial (NCT06643767) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Abilene research site is actively enrolling participants for this clinical trial. You'll receive care from experienced breast cancer specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all breast cancer clinical trials near you to find additional studies recruiting in your area.

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