Actively Recruiting
Brass Mesh Bolus in Rotational Post-Mastectomy Radiation Therapy
Led by Nova Scotia Cancer Centre · Updated on 2024-05-22
20
Participants Needed
1
Research Sites
96 weeks
Total Duration
On this page
Sponsors
N
Nova Scotia Cancer Centre
Lead Sponsor
H
Hannah Dahn
Collaborating Sponsor
AI-Summary
What this Trial Is About
The hypothesis is that the daily use of brass mesh bolus achieves a comparable dose to every-other-day use of Superflab bolus (current standard of care) in chest wall post-mastectomy patients treated with rotational 6 MV photon delivery.
CONDITIONS
Official Title
Brass Mesh Bolus in Rotational Post-Mastectomy Radiation Therapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women undergoing rotational chest wall radiotherapy following mastectomy for breast cancer treatment who would utilize Superflab bolus on some, but not all, days of radiotherapy treatment.
You will not qualify if you...
- Patients who require daily bolus due to skin involvement or other high-risk features requiring a high skin dose will not be included.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Nova Scotia Health Authority
Halifax, Nova Scotia, Canada, B3H 1V7
Actively Recruiting
Research Team
H
Hannah Dahn, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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