Actively Recruiting
Optimal Mammography View Sequencing in Women With a History of Breast Cancer Undergoing Surveillance Mammography
Led by Royal College of Surgeons, Ireland · Updated on 2026-03-02
400
Participants Needed
1
Research Sites
253 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This prospective, single-centre, parallel-group randomised controlled trial evaluates the optimal sequencing of mammography views in women with a history of breast cancer undergoing surveillance mammography. Women treated with breast-conserving surgery within the previous five years will be randomised 1:1:1:1 to one of four mammography view sequencing groups. The primary objective is to compare patient-reported pain and satisfaction across sequencing groups. Secondary objectives include comparison of image quality (PGMI scoring), compression force, and breast thickness. A total of 400 participants will be enrolled at Beaumont Hospital Breast Care Centre over 2.5 years.
CONDITIONS
Official Title
Optimal Mammography View Sequencing in Women With a History of Breast Cancer Undergoing Surveillance Mammography
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female patients aged 18 years or older
- History of breast cancer treated with breast-conserving surgery (wide local excision)
- Undergoing first annual surveillance mammogram following completion of surgery and radiotherapy
- Within five years of breast cancer treatment
- May have history of whole-breast or partial-breast radiotherapy
- May have history of axillary surgery
- Able and willing to provide informed consent
You will not qualify if you...
- Male patients
- Patients younger than 18 years
- History of mastectomy
- History of bilateral wide local excision
- Lack of capacity to provide informed consent
- More than five years since completion of breast cancer treatment
AI-Screening
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Trial Site Locations
Total: 1 location
1
Beaumont RCSI Cancer Centre
Beaumont, Dublin, Ireland, D09V2N0
Actively Recruiting
Research Team
P
Prof Nuala Healy
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
4
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