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A study to evaluate Enhanced Visual Assessment System in detecting cervical cancer

To evaluate a low â??cost efficient and effective Enhanced Visual Assessment System developed by Mobile ODT on the basis of ease of use, affordability, increased revenue to offset cost and patient / provider satisfaction.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/03/008128
Enrollment
2000
Registered
2017-03-17
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Mobile ODT Mobile Optical Detection Technologies
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Able to understand and consent to participating in the study

Exclusion criteria

Exclusion criteria: Women previously detected with cervical cancer

Design outcomes

Primary

MeasureTime frame
Patients detected with cervical cancer / precancerous reasonsTimepoint: 6 months—

Secondary

MeasureTime frame
Provider and patient satisfaction with EVA System, consistent with utilization of the deviceTimepoint: 6 months—

Countries

India

Contacts

Public ContactMr Vibhav Gupta

International Oncology Services Pvt Ltd

dior.kara@iosplcancer.com9920099156

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026