Mastectomy Clinical Trials

Clinical trials related to Mastectomy Procedure

Margin Optimisation Using Z-axis Assessment With Real-time Tomosynthesis (MOZART Study).

Status: Recruiting
Location: See location...
Intervention Type: Procedure, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Breast-conserving surgery is commonly performed to remove early-stage breast cancer or ductal carcinoma in situ (DCIS). During surgery, the goal is to completely remove the tumour with a clear margin of normal tissue around it. If cancer cells are found at the edge of the removed tissue (a positive margin), patients may need a second operation (re-excision). Re-excision can delay further treatment, increase patient anxiety, and increase healthcare costs. To help assess margins during surgery, surgeons use specimen imaging. Standard practice involves two-dimensional (2D) specimen mammography, usually performed in the radiology department. This requires temporary transfer of the specimen out of the operating theatre and provides limited depth information. The MOZART study is evaluating whether three-dimensional (3D) digital breast tomosynthesis, performed in the operating theatre using the Mozart system, improves margin assessment compared to standard 2D specimen mammography. Patients undergoing breast-conserving surgery at Beaumont Hospital who agree to participate will be randomly assigned (like flipping a coin) to one of two groups: Standard 2D specimen mammography (current standard practice), or 3D digital breast tomosynthesis performed in theatre. In both groups, the operating surgeon will review the images during surgery and decide whether additional tissue needs to be removed. The final margin status will be determined by routine laboratory analysis after surgery. The main goal of this study is to compare the rate of positive margins between the two imaging methods. Other outcomes include the need for additional surgery, operating time, and overall workflow efficiency. The results of this study may help determine whether intraoperative 3D imaging improves surgical outcomes and reduces the need for re-excision in patients undergoing breast-conserving surgery.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: t
View:

• Female patients

• Age ≥ 18 years

• Diagnosis of primary invasive breast cancer or ductal carcinoma in situ (DCIS)

• Planned breast-conserving surgery with curative intent

• No clinical or radiological evidence of distant metastatic disease at time of recruitment

• Able to provide written informed consent

• Fluent in English (spoken and written)

Locations
Other Locations
Ireland
Beaumont RCSI Cancer Centre
RECRUITING
Beaumont
Contact Information
Primary
Prof Arnold Hill, MB, BCh, BAO, MCh, FRCSI
adkhill@rcsi.com
018093000
Backup
Aisling Hegarty, PhD
Aislinghegarty@rcsi.ie
Time Frame
Start Date: 2025-12-18
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 314
Treatments
Active_comparator: Standard 2D Speciman Mammography (Control)
Participants undergo intraoperative specimen imaging using standard two-dimensional (2D) specimen mammography performed in the radiology department following tumour excision. The operating surgeon reviews the images intraoperatively to assess margin adequacy and determines whether additional excision is required prior to wound closure. All other aspects of surgical care follow standard institutional practice.
Experimental: 3D Digital Breast Tomosynthesis (Mozart System Intervention)
Participants undergo intraoperative specimen imaging using three-dimensional (3D) digital breast tomosynthesis with the Mozart 3D Specimen Radiography System, performed directly in the operating theatre. The operating surgeon reviews reconstructed tomosynthesis images in real time to assess margin adequacy and determine whether additional excision is required prior to wound closure. All other aspects of surgical care remain unchanged.
Related Therapeutic Areas
Sponsors
Leads: Royal College of Surgeons, Ireland

This content was sourced from clinicaltrials.gov