Role Of Colposcopy In Evaluation Of Suspicious Cervix

NCT ID: NCT06673680

Last Updated: 2024-11-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

53 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-10-01

Study Completion Date

2025-05-30

Brief Summary

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do colposcopy and cervical punch biopsy then compare between findings

Detailed Description

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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.

Conditions

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Cancer Cervix

Study Design

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Observational Model Type

CASE_CROSSOVER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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colposcopic evaluation

do colposcopy and cervical punch biopsy then compare between findings

Do colposcopy and cervical punch biopsy then compare between findings

Intervention Type 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.

Interventions

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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.

Intervention Type DEVICE

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Sohag University

OTHER

Sponsor Role lead

Responsible Party

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Omar Kamal Mohamed

Resident

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Hazem A prof, MD

Role: STUDY_DIRECTOR

Sohag university hospitals

Locations

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Sohag university Hospital

Sohag, , Egypt

Site Status RECRUITING

Countries

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Egypt

Central Contacts

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Omar K Mohamed, master

Role: CONTACT

+201022827251 ext. +201225889053

Mohamed K engineer, Master

Role: CONTACT

+201027836607 ext. +201225889053

Facility Contacts

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Magdy M Amin, professor

Role: primary

Other Identifiers

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colposcopy in cancer cervix

Identifier Type: -

Identifier Source: org_study_id

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