None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Age up to and above 18 years 2.Ability to understand and the willingness to sign a written informed consent document.
Exclusion criteria
Exclusion criteria: 1.Unwilling to provide consent. 2.Prior history of oral cancer 3.Concomitant physical or mental disability precluding ability to comply with study protocol requirements 4.Suspected/confirmed infectious diseases/conditions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the feasibility practicality compliance and satisfaction of community based oral cancer screening.To assess the ability to acquire high quality visual images and tissue biopsies samples on the study cohort as per protocol. To identify oral mucosal lesions requiring biopsy through a screening examination augmented by FV. Lesions will be categorized as either negative with known cause no clinical concerns or positive clinically suspect cancer or precancer. Timepoint: 1 year from 01/03/2018 to 28/2/2019 | — |
Secondary
| Measure | Time frame |
|---|---|
| One hundred participants will provide the research team with sufficient experience to assess the study protocol CRFs and issues such as patient flow participants and lesion assessment and management to fine tune the cohort studyTimepoint: six months to one year | — |
Countries
India
Contacts
MNJ Institute of Oncology and Regional Cancer Centre