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Trial Title:
Screening for Early Cervical Cancer Detection
NCT ID:
NCT06550583
Condition:
Cervical Cancer
Cervix Neoplasm
Conditions: Official terms:
Uterine Cervical Neoplasms
Study type:
Observational
Overall status:
Active, not recruiting
Study design:
Time perspective:
Cross-Sectional
Intervention:
Intervention type:
Diagnostic Test
Intervention name:
Pap smear /Test
Description:
Patients will be placed in the lithotomy position, and a sterile bivalve speculum will be
inserted into the vagina.
• A sample will be taken from the ectocervix by rotating a wooden Ayre spatula 360°. The
sample will be quickly smeared onto a labeled glass slide and fixed with 95% ethyl
alcohol in a jar to be sent to the Department of Pathology for cytopathological
examination
Summary:
This study is to audit results and adherence to Cervical Screening program before and
after the implementing awareness of the WHO guidelines of screening among the
multidisciplinary healthcare workers and patients.
Detailed description:
Cervical cancer screening is the asymptomatic detection of pre-cancer and cancer in women
at risk, with at least one screening suggested for women aged 30-49 years. According to
the World Health Survey (2015), 19% of eligible women in developing countries and 63% of
those in developed nations had their cervical cancer screening done using a Pap smear or
visual inspection with acetic acid (VIA).
According to latest estimates by World Health Organization (WHO), in Egypt, 866 women are
diagnosed with cervical cancer every year and 373 die from the disease. Cervical cancer
is the 13th most common cancer in women in Egypt and the 10th most common cancer in women
aged between 15 to 44 years . Statistics from Egyptian studies provide pre invasive
cervical lesion incidence levels of 0.3 % to 0.5 % .
The human papillomavirus (HPV) is one of the most significant risk factors for cervical
cancer. HPV can be transmitted through sexual contact, including vaginal or oral sex with
an infected person. HPV has more than 100 strains, of which HPV16 and HPV18 account for
about 70% of invasive cervical cancers
Criteria for eligibility:
Study pop:
Female patients who will attend gynecology clinics at Women & Children Hospital in
reproductive age in (Assuit) Egypt
Sampling method:
Probability Sample
Criteria:
Inclusion Criteria:
- Women 20-60 years.
- Sexually active.
- Fulfilling Cervical Check's eligibility criteria for screening at the time of
the audit
https://www.cervicalcheck.ie/_fileupload/File/Eligibility%20Framework.pdf
Exclusion Criteria:
Patient who had underwent to total hysterectomy.
- Pregnant or postpartum or post abortive patients
- Patient having any history of treatment for cervical dysplasia.
- Immunocompromised patients.
Gender:
Female
Gender based:
Yes
Gender description:
sexually active women in reproductive age .
Minimum age:
20 Years
Maximum age:
60 Years
Locations:
Facility:
Name:
Assiut University
Address:
City:
Assiut
Zip:
71111
Country:
Egypt
Start date:
June 1, 2023
Completion date:
September 30, 2024
Lead sponsor:
Agency:
Assiut University
Agency class:
Other
Source:
Assiut University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06550583