See and Treat in an Outpatient Setting in Women Above 45 Years With Cervical Dysplasia

Cervical Dysplasia Clinical Trial

Official title:

See and Treat in an Outpatient Setting in Women Above 45 Years With Cervical Dysplasia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04298957
• Other study ID #: 172230
• Status: Completed
• Phase: N/A
• Start date: March 13, 2019
• Est. completion date: January 31, 2022

Study information

• Verified date: April 2021
• Source: University of Aarhus
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study will investigate if implementation of "see and treat" in the outpatient clinic can optimize the diagnosis, clinical follow-up and treatment of older women with positive cervical screening test.

Description:

In Denmark, 370 women are diagnosed with cervical cancer every year and approximately 100 women die from the disease. Young women can be protected with the HPV vaccine, but it will take decades before the vaccine has an effect on older women. Women who are HPV positive have a risk of developing severe dysplasia of 25-55% within 10 years. Compared to younger women, older women are also more likely to be diagnosed with advanced-stage disease and their mortality is high. Due to retraction of the transformation zone into the cervical canal and atrophy of the mucosa the performance of colposcopy is low. Furthermore, the sensitivity of cytology decreases with age. This makes it very difficult to obtain sufficient biopsies and therefore postmenopausal women are often required to undergo colposcopy two to three times. Waiting for a final diagnosis and treatment not only has a large mental and practical impact on the women themselves, but it is also an economic burden for the health care system.

"See and treat" is a procedure that involves cervical cytology and HPV test, a colposcopy, cervical biopsies, and finally a loop electrosurgical excisional procedure by which the transformation zone is removed. This approach allows women to be diagnosed and treated in one visit.

In this project, the aim is to investigate if the implementation of "see and treat" in a gynecological outpatient clinic can optimize the diagnostics, clinical follow-up, and treatment of older women with abnormal cervical cytology or HPV-infection.

Participants Women aged ≥ 45 years with cervical dysplasia and/or a positive HPV test are referred from the general practitioner to the gynecological department.

Procedure At each inclusion site, the local project manager evaluates all the referred women for possible inclusion. Project information is sent either by e-mail or letter to eligible women. At the outpatient clinic, the eligible women will be informed about the project and asked to sign an informed consent form regarding their participation in the project.

If the eligible women agree to participate a physician in the outpatient clinic will obtain a cervical smear (i.e. cytology and Human Papillomavirus (HPV) test) and perform colposcopy and take four random biopsies. If the transformation zone (TZ) is partly visible or not visible a cone biopsy will be performed in local anesthesia (Citanest).

If the participant meet the exclusion criteria or declines to participate standard treatment will be offered (colposcopy and biopsies).

The included patients will be followed up with an HPV test after 6 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 109
• Est. completion date: January 31, 2022
• Est. primary completion date: June 30, 2021
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 45 Years and older

Eligibility

Inclusion Criteria:

• Women = 45 years with a positive screening test (abnormal cytology and/or persistence HPV positive) who are referred to the Department of Obstetrics and Gynecology.

• Type 2 or 3 transformation zone (a partly or invisible transformation zone).

Exclusion Criteria:

• Type 1 transformation zone (fully visible)

• Current or previous diagnosis of cervical cancer.

• Pregnancy or pregnancy wish.

• Previously cone biopsy

Related Conditions & MeSH terms

• Cervical Dysplasia
• Cervical Intraepithelial Neoplasia
• Cervical Lesion
• Cervix Disease
• Uterine Cervical Diseases
• Uterine Cervical Dysplasia

Intervention

Procedure:
• Cone biopsy
Cone biopsy if transformation Zone (TZ) 2 or TZ 3

Locations

Country	Name	City	State
Denmark	Horsens Regional Hospital	Horsens	Jutland
Denmark	Randers Regional Hospital	Randers	Jutland
Denmark	Viborg Regional Hospital	Viborg	Jutland

Sponsors (1)

Lead Sponsor	Collaborator
University of Aarhus

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cervical intraepithelial neoplasia = grade 2 (CIN2+) lesion after referral with a positive cervical screening test	The prevalence of CIN2+ lesions in women =45 years included in the study	The histological diagnose from the Pathological Department will be available 8 weeks after inclusion.
Primary	Concordance between cytology and histology	Concordance between cytology, biopsies and cone biopsy in the ability to detect CIN2+ changes	The histological diagnose from the Pathological Department will be available 8 weeks after inclusion.
Primary	Clearance of HPV	Clearance rate of HPV after 6 months	This will be available 7 months after inclusion.
Primary	Complication rate	Complication rate of bleeding, infection and/or stenosis	Complication rate will be evaluated 6 months after inclusion.