Overview

Wide-Field and High Resolution In Vivo Imaging in Visualizing Lesions in Patients With Oral Neoplasia Undergoing Surgery

Status:
Recruiting
Trial end date:
2021-12-31
Target enrollment:
0
Participant gender:
All
Summary
This clinical trial studies wide-field and high resolution in vivo imaging in visualizing lesions in patients with abnormal or uncontrolled oral cell growth (neoplasia) undergoing surgery. Diagnostic procedures, such as wide-field and high resolution in vivo imaging, are devices that let researchers look at a wide area of the lining of the mouth by shining different colors inside the mouth and taking pictures and this may help doctors to decide if a mouth lesion has a high risk of being pre-cancerous or cancerous.
Phase:
Early Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
M.D. Anderson Cancer Center
Collaborators:
National Cancer Institute (NCI)
National Institutes of Health (NIH)
Treatments:
Proflavine
Criteria
Inclusion Criteria:

- Adult subjects with oral lesions undergoing surgical resection (i.e., only patients
who are scheduled to undergo a surgery of the head & neck area to remove or biopsy
oral lesions will be eligible to participate in the study); patients with previous
treatment are eligible

- Ability to understand and the willingness to sign a written informed consent document
(ICD)

Exclusion Criteria:

- Known allergy to proflavine or acriflavine

- Pregnant or nursing females

- The participant will be excluded from participation in another clinical research trial
(i.e., a trial in which an agent is actively administered to the study subject), while
being imaged (on active treatment) on this protocol