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Radiation Therapy
Brass Mesh Bolus for Breast Cancer
N/A
Recruiting
Research Sponsored by Nova Scotia Cancer Centre
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 1 year
Awards & highlights
Study Summary
This trial tests if daily use of a brass mesh bolus can replace the current standard of care for chest wall radiation after mastectomy.
Eligible Conditions
- Breast Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, an average of 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Skin Dose Enhancement Under Brass Mesh Bolus
Trial Design
1Treatment groups
Experimental Treatment
Group I: Post-Mastectomy Radiation Therapy PatientsExperimental Treatment1 Intervention
Any patient who is going through radiation to their chest wall following mastectomy using a rotational delivery technique and 6 MV, and uses Superflab bolus for some but not all fractions of radiotherapy
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Who is running the clinical trial?
Michael KucharczykUNKNOWN
Hannah DahnUNKNOWN
Nova Scotia Cancer CentreLead Sponsor
4 Previous Clinical Trials
151 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- Patients who need frequent injections or have severe skin problems will not be included.
Research Study Groups:
This trial has the following groups:- Group 1: Post-Mastectomy Radiation Therapy Patients
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
How extensive is the scope of this experiment in terms of participant numbers?
"Affirmative. According to clinicaltrials.gov, this trial has been open for recruitment since January 18th 2023 and is actively recruiting participants now. The study seeks to enroll a total of 20 patients at one medical site."
Answered by AI
Are there vacancies in this medical experiment for new participants?
"Affirmative. According to clinicaltrials.gov, this experiment is pursuing subjects at the present time; it was initially published on January 18th 2023 and revised more recently on July 22nd 2023. This medical trial requires a total of 20 volunteers from one location."
Answered by AI
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