Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

Mammography Texture Features in Women and AI

Official title: A Cohort Study on feMale Patients' mammogRaphic texturE featureS: the COMPRESS Trial

Run by Tampere University Hospital · NCT06469606 · Data updated 2026-11-12

This study tests an AI tool to help interpret mammograms for women needing mastectomy.

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment200 (estimated)
SponsorTampere University Hospital
Academic / other
Locations1 site (Tampere)
StatusRecruiting
StartedJune 17, 2024
Main results expectedDecember 15, 2035
Study endsDecember 15, 2038
Registry record updatedAugust 5, 2026
Trial IDNCT06469606 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Biological females aged 18 or older with a clinical indication for unilateral or bilateral mastectomy who can provide informed consent.

Probably not a fit

Patients without an indication for mastectomy or those unable to benefit from AI-assisted interpretation may not experience direct benefits.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study investigates how radiomics texture features from mammography relate to clinical and biological factors in female patients. It uses an AI-based tool to support clinical decision-making in the context of mastectomy indications. The goal is to understand how imaging parameters and biology influence texture features and to translate these findings into robust AI-assisted practice. The study will examine the interplay between imaging, clinical data, and biology to improve consistency and usefulness of AI outputs. No phase information is provided for this intervention.

Why it matters

Potential benefit: If successful, the AI tool could improve consistency and accuracy of mammography interpretation to guide treatment decisions.

How similar studies have gone: Previous radiomics studies in mammography have shown promise in risk assessment and lesion detection, but translation to routine practice remains challenging and is under active investigation.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Candidate is a biological female aged 18 years or above;
* Candidate is willing and able to give informed consent and gives their written consent for the participation in the study;
* There is a clinical indication for a uni- or bilateral mastectomy

Exclusion Criteria:

* Candidate lacks the capacity to provide informed consent;
* Candidate has breast implants

Where it's running

  • Wellbeing Services County of Pirkanmaa
    Tampere, Finland
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.