A clinical trial to detect cervical cancer at early stage with light based hand held device.
Not Applicable
- Conditions
- Health Condition 1: null- Primary health condition(s): Female patients with abnormal Pap smear findings and have probability of cervical cancer / pre-cancer.
- Registration Number
- CTRI/2017/09/009886
- Lead Sponsor
- Impacting Research Innovation and Technology India
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult and elderly female patients with sign & symptoms (such as abnormal vaginal bleeding, An unusual discharge from the vagina, pelvic pain etc.)
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Co- and cross-polarized fluorescence and elastic scattering spectra. <br/ ><br> <br/ ><br>Timepoint: 15 â?? 20 minute measurement time. <br/ ><br>
- Secondary Outcome Measures
Name Time Method Different parameters to discriminate different grades of pre-cancer / cancer. <br/ ><br>Timepoint: Within 1 hr after measurements <br/ ><br>