Role Of Colposcopy In Evaluation Of Suspicious Cervix

ConditionCancer Cervix
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-60
SponsorSohag University

About this trial

do colposcopy and cervical punch biopsy then compare between findings

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Design model

Case-crossover

Time perspective

Cross-sectional

Treatments tested in this trial

  • Do colposcopy and cervical punch biopsy then compare between findings

    Device

    The 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

53 Participants
are divided into 1 treatment group
Group A: colposcopic evaluation1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.