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Efficacy of mixed reality assisted partial mastectomy

Efficacy of Image-Guided Techniques in Breast-Conserving Surgery for Early Breast Cancer. Phase 2 Study. - MRAPM

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1040240075
Enrollment
10
Registered
2024-08-21
Start date
2024-08-21
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 cancer

Interventions

Overview of the Surgical Technique Technology: Image-guided technology (VINCENT by FUJIFILM, head-mounted device HoloLens 2 by Microsoft). Procedure: Breast-conserving surgery is performed, with rese

Sponsors

Hirofumi Terakawa
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1) Disease and Diagnostic Methods - Disease: Early-stage breast cancer. - Diagnostic Methods: Diagnosis is made in accordance with the "Breast Cancer Treatment Guidelines, 8th Edition," using mammography, ultrasound, and, if necessary, MRI or biopsy. 2) Stage and Type of Cancer - Stage: Stage I or Stage II breast cancer. 3) Age - Age: Patients aged 20 years or older. 4) Sex - Sex: Female. 5) Performance Status - Performance Status (ECOG):Patients with an ECOG performance status of 1 or lower. 6) Written Consent from Patients - Written Consent: Patients who have provided written consent to participate in this study after receiving sufficient informed consent and of their own free will.

Exclusion criteria

Exclusion criteria: 1) Patients who have participated in other clinical trials (including drug trials) within the past 3 months. 2) Patients who are receiving preoperative hormone therapy (such as oral anastrozole) or preoperative chemotherapy. 3) Patients with significant comorbidities (such as heart failure, progressive liver or kidney disease, severe diabetes, etc.). 4) Patients whom the principal investigator or sub-investigator deems inappropriate for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Surgical Time, Blood Loss, Secondary Additional Resection

Secondary

MeasureTime frame
cancer-positive at the edge of the breast tissue margin

Contacts

Public ContactMohri Ryosuke

Department of Breast Surgery, Kanazawa Univercity Hospital

brigantin51@gmail.com+81-76-265-2261

Outcome results

None listed

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