Oral cancer detection in rural region using multiple devices
Not Applicable
- Conditions
- Health Condition 1: K132- Leukoplakia and other disturbancesof oral epithelium, including tongueHealth Condition 2: K135- Oral submucous fibrosis
- Registration Number
- CTRI/2024/03/064717
- Lead Sponsor
- ational Institute of Dental and Craniofacial research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1 Age 18 or above
2 Willing and able to consent to the study
3 Presenting or diagnosed with any oral lesion, indicated for biopsy based on lesion and other health status
Exclusion Criteria
1 Currently undergoing treatment for any malignancy.
2 Presence of tuberculosis or any other acute illness
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Multimodal intra oral imaging system with sensitivity and specificity more than 90% for oral cancer and benign or healthy <br/ ><br>Multimodal intra oral imaging system with sensitivity and specificity more than 85% for oral pre cancer and benign or healthy <br/ ><br>Multimodal intra oral imaging system with sensitivity and specificity more than 90% for oral cancer and benign or healthy <br/ ><br>Multimodal intra oral imaging system with sensitivity and specificity more than 80% for non neoplastoc from benign oral cancer and pre cancerTimepoint: 5 years
- Secondary Outcome Measures
Name Time Method clinical feasibility of the prototyped intraoral imaging systemTimepoint: every 2 weeks