Data collection for a breast ultrasonic imaging device

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCTs032200416

Enrollment

200

Registered

2021-03-12

Start date

2021-03-23

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast diseases

Interventions

Breast imaging using a device

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1)Female, Age 20 or older at the time of consent acquisition 2)A person who has obtained an informed consent with sufficient explanation to participate in this study 3)Those who are planning to have breast surgery and can have a ring echo examination before breast surgery

Exclusion criteria

Exclusion criteria: 1) Unable to get on and off the device by oneself or unable to lay prone on the device for 30 minutes 2)Pregnant women or women who are capable of pregnancy 3)Patients who had heart pacemaker or implantable cardioverter defibrillator 4)Judged by a doctor to be in a condition inappropriate for the participation in the study

Design outcomes

Primary

Measure	Time frame
Evaluation of image	—

Secondary

Measure	Time frame
1)Evaluation of image 2)Patient safety and comfort	—

Contacts

Public ContactHidemi Furusawa

Breast surgical oncology clinic, Kawaguchi kogyo general hospital

hidemi.furusawa@kogyohsp.gr.jp+81-48-229-0707

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026