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Study identifier: NCT07116642 Synced from ClinicalTrials.gov · July 28, 2026
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Comparing Patient Reported Outcomes and Clinical Outcomes Based on Different Scar Placement in Patients Undergoing Standard Breast Conserving Surgery for Breast Cancer: The PROM-S Study.

Condition: Breast Cancer - Female · Surgery of Breast Cancer  ·  Sponsor: The Leeds Teaching Hospitals NHS Trust

PhaseN/A
Planned participants100
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is for patients with breast cancer and the objective is to compare patient reported outcome measures (PROMs) based on scar placement in patients undergoing standard breast-conserving surgery (sBCS). BCS has become the standard of care for eligible patients with breast cancer (current UK national BCS rate is 60%). Scar placement for sBCS can be divided into two groups: those directly over the cancer, or those in remote locations (e.g. around the nipple, near the armpit, the lower part of the breast, where the breast and the chest meet etc.) with the aim of hiding the scar in more visually acceptable locations on the breast. Multiple factors determine where the scar is placed such as aesthetics, other health conditions, location of the cancer, etc. However, it is currently unclear whether the location of scar placement for sBCS affects patient reported outcomes. The growing importance on breast cosmesis has led to more attention from clinicians and patients with regards to the selection of surgical incision placement for sBCS. By using a validated questionnaire (BREAST-Q), we wish to assess if there is any difference in PROMs based on scar placement (over the lesion vs. remote) in patients undergoing sBCS. It is anticipated that the study results will help champion and guide care for future breast cancer patients, as well as providing an insight into how patient satisfaction may vary between different sBCS approaches. This questionnaire study will include consecu…

This description comes directly from the study's public registry record.

Talk to the study team

Sue M Dr Hartup, PhD, RGN  ·  +44 0113 2068628  ·  s.hartup@nhs.net

Baek Mr Kim, FRCS, MD, MA  ·  +44 0113 2068628  ·  b.kim@nhs.net

Always discuss trial participation with your own doctor first.

Locations (1)

St James's University HospitalLeeds, West Yorkshire, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT07116642