About this trial
do colposcopy and cervical punch biopsy then compare between findings
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age from 30 to 64 years old.
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
Disqualifiers
Pregnant women
Women having active vaginal bleeding.
Any past treatment for cervical lesions.
Women having frank growth of cervix.
Trial population
* Age from 30 to 64 years old. * 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.
Trial design
Case-crossover
Cross-sectional
Treatments tested in this trial
Do colposcopy and cervical punch biopsy then compare between findings
DeviceThe aim of this study is to correlate colposcopy and histopathological findings in early screening of suspicious cervix and cervical cancer. And to do a colposcopic evaluation of all cervical lesions and the early detection of all cervical precancer and invasive lesions of the cervix in symptomatic women.
Treatment groups
Trial outcomes
Primary outcomes
comparison between colposcopic findings of suspicious cervix and histopathologic findings
Correlate colposcopy and histopathological findings in early screening of suspicious cervix and cervical cancer. And to do a colposcopic evaluation of all cervical lesions and the early detection of all cervical precancer and invasive lesions of the cervix in symptomatic women.
Sponsors and contacts
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