VIA Versus Colposcopy (NCT07692919) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
VIA Versus Colposcopy
200 participantsStarted 2026-08-01
Plain-language summary
The aim of this study is to compare the effectiveness of visual inspection with acetic acid (VIA) versus colposcopy in terms of sensitivity and specificity in diagnosis of pre-malignant cervical lesions among women, and to assess the awareness of women regarding cervical cancer screening methods.
Who can participate
Age range
25 Years – 65 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age from 25 to 65 years.
* Patient undergoing cervical cancer screening using VIA and colposcopy.
* Women with symptoms such as white discharge, post-coital bleeding, and intermenstrual bleeding.
* Women with the clinically unhealthy cervix (erosion, bleeding on touch, simple leukoplakia, keratinization)
* Women with Pap smear showing dysplasia.
Exclusion Criteria:
* • Pregnant women (if VIA or colposcopy is contraindicated).
* Women with obvious invasive cervical cancer diagnosed previously.
* Women who refuse to provide informed consent or are unable to cooperate with the examination.
* Women having active vaginal bleeding.
* Any past treatment for cervical lesions.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
VIA Versus Colposcopy in terms of in terms of sensitivity and specificity
Timeframe: 2 weeks
2
sensitivity and specificity in diagnosis of pre-malignant cervical lesions among women
Timeframe: From enrollment to the the result at 14 days