Health Condition 1: null- Patients with suspected cervical cancer/ precancerous lesions
Conditions
Interventions
Intervention1: Single arm, non-randomized trial: non-randomized trial
Intervention2: Cervical cancer detection: Diffuse reflectance imaging and fluorescence and diffuse reflectance point monitoring te
Sponsors
Centre for Earth Science Studies
Eligibility
Inclusion criteria
Inclusion criteria: Patients with positive pap smear reports Patients referred for colposcopic examination Patients with any kind of clinically suspecting lesions in the uterine cervix
Exclusion criteria
Exclusion criteria: Patient refusal Patients with transmittable diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identification of the malignant site for optimal biopsy and histology; and Reduction of false negativesTimepoint: First arrival at OP clinic | — |
Secondary
| Measure | Time frame |
|---|---|
| Reduced trauma, morbidity; and Real-time, Noninvasive diagnosisTimepoint: At the first visit to Clinic | — |
Countries
India
Contacts
Public ContactDr N Subhash
Vinvish Technologies
Outcome results
None listed