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Procedure
da Vinci Surgical System Model IS4000 for Head and Neck Squamous Cell Carcinoma (FIND Trial)
N/A
Waitlist Available
Led By John de Almeida, MD
Research Sponsored by University Health Network, Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age >= 18
Metastatic squamous cell carcinoma (T0,N1-3,M0) to at least one regional lymph node of the neck (includes N1-N3) based on fine needle aspiration (FNA) biopsy, core biopsy, excisional biopsy, or neck dissection
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years
Awards & highlights
FIND Trial Summary
This trial is testing a new way to find small mouth and throat cancers using a robot. If it works, it could help reduce side effects from treatment.
Eligible Conditions
- Head and Neck Squamous Cell Carcinoma
FIND Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowFIND Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Determination of the rate of out-of-field failures following treatment
Secondary outcome measures
Adverse Events (AE) monitoring
Determination of patterns of failure by location
Determination of proportions of occult oropharyngeal cancers identified
+8 moreFIND Trial Design
1Treatment groups
Experimental Treatment
Group I: da Vinci Surgical System Model IS4000Experimental Treatment1 Intervention
Transoral robotic surgery, followed by tailored radiotherapy
Find a Location
Who is running the clinical trial?
University Health Network, TorontoLead Sponsor
1,468 Previous Clinical Trials
484,468 Total Patients Enrolled
John de Almeida, MDPrincipal InvestigatorUniversity Health Network, Toronto
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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