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Recruiting NCT06673680

Role Of Colposcopy In Evaluation Of Suspicious Cervix

Observational Cancer Cervix

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Do colposcopy and cervical punch biopsy then compare between findings.
Who it may be relevant to
Registry conditions: Cancer Cervix. Basic parameters: 18 years — 60 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

do colposcopy and cervical punch biopsy then compare between findings

Detailed description

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.

Interventions

  • Device Do colposcopy and cervical punch biopsy then compare between findings
    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.

Primary outcome measures

  • comparison between colposcopic findings of suspicious cervix and histopathologic findings [Time frame: baseline]

Eligibility criteria

Inclusion criteria

  • 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

Exclusion criteria

  • Pregnant women
  • Women having active vaginal bleeding.
  • Any past treatment for cervical lesions.
  • Women having frank growth of cervix.
  • Women who underwent a hysterectomy.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-crossover

Study locations

Egypt · 1 center
  • Sohag university Hospital — Sohag

Identifiers

NCT: NCT06673680 · colposcopy in cancer cervix

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗