Actively Recruiting
Laser Speckle Imaging During Breast Reconstruction
Led by Royal Devon and Exeter NHS Foundation Trust · Updated on 2024-07-26
60
Participants Needed
1
Research Sites
53 weeks
Total Duration
On this page
Sponsors
R
Royal Devon and Exeter NHS Foundation Trust
Lead Sponsor
U
University of Exeter
Collaborating Sponsor
AI-Summary
What this Trial Is About
Around 3500 women a year have surgery to reconstruct a breast/s after cancer. Breast reconstruction can have a positive impact on their lives, but unfortunately 3 or 4 in 10 women have problems with healing after their operation. This is distressing and often leads to more medical care or surgery. These problems are often caused by poor blood flow to the skin and deeper tissues used to reconstruct the breast. The investigators have developed a new device that does not touch the skin and provides immediate, continuous images of skin blood flow (the flow that surgeons cannot see). To test this device the investigators took images of blood flow during breast reconstruction surgery. The investigators found that imaging was good at showing where skin blood flow was poor and led to problems with healing and where flow was good and there were fewer problems after surgery (from minor problems, e.g. delayed healing; to major problems, e.g. loss of new breast). The investigators think this device can help surgeons choose healthy skin during breast reconstruction and so help more patients to heal without surgical problems. The investigators need to test the new imaging device in a large clinical trial to find out how effective it is at improving healing for women after breast reconstruction. Before this, the investigators need to find out if such a trial is possible and acceptable to patients, theatre staff and surgeons. The investigators will recruit 60 women who are having breast surgery and will randomly choose 30 to have surgery without blood flow imaging and 30 to have surgery with blood flow imaging. The investigators will follow up the women whilst in hospital and for the following 6 months to record any problems. In particular the investigators need to find out how many patients will volunteer for the study and the study can collect all the information needed during the 6 months after surgery. The results from this study will be used to plan a much larger clinical trial that will test whether blood flow imaging is effective, improves patient recovery after surgery and provides good value for money for the NHS.
CONDITIONS
Official Title
Laser Speckle Imaging During Breast Reconstruction
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female, aged 18 or over
- Able and willing to provide informed consent
- Scheduled for breast reconstruction by autologous free flap surgery (either immediately post-mastectomy or delayed)
You will not qualify if you...
- Unable to give written informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Royal Devon University Healthcare NHS Foundation Trust
Exeter, Devon, United Kingdom, EX2 5DW
Actively Recruiting
Research Team
L
Lucy Gates, PhD
CONTACT
A
Angela Shore
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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