COOL-IT-PRO: Cryoablation for Breast Cancer in Non-surgical Patients

This study, called COOL-IT-PRO, is looking at the safety of a treatment called cryoablation for breast cancer. Cryoablation uses extreme cold to destroy cancer cells. This study is for people with breast cancer who cannot have surgery because of other medical conditions, or if surgery isn't recommended for other reasons. You can join if you are 18 or older, have a breast cancer diagnosis, and your tumor can be seen on an ultrasound and is more than 5mm from your skin. The main goal is to see how many patients experience serious treatment-related problems over three years. The study status is currently unclear, and it plans to include 100 participants.

Study design
This is an observational study, meaning researchers will collect information from patients who receive cryoablation. It is a registry study, gathering data on 100 planned participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for up to three years to monitor for any serious treatment-related complications.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05972343

COOL-IT-PRO: Cryoablation of Breast Cancer in Non-surgical Patients

Recruiting
Not specifiedAges 18+Observational
Washington University School of Medicine
~100 participants
Updated 2026-05-07 on ClinicalTrials.gov
What's tested:Cryoablation

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Proportion of patients who are free of serious treatment related complications per CTCAE v 5.0
Measured over Through 3 year follow-up
Breast Cancer
Cancer of the Breast
1 sites across 1 states
Missouri1
  • Heather Garrett, M.D. · PRINCIPAL_INVESTIGATOR · Washington University School of Medicine

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  • Proportion of patients who are free of serious treatment related complications per CTCAE v 5.0Through 3 year follow-up