Actively Recruiting
Improving Diagnostics in Cervical Dysplasia
Led by University of Aarhus · Updated on 2024-12-10
150
Participants Needed
1
Research Sites
99 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Cervical cancer is the fourth most common cancer in women worldwide. It is caused by an infection with human papillomavirus (HPV). A persistent infection with HPV is associated with increased risk of precancerous lesions, which may further develop into cervical cancer. To reduce the disease burden, accurate and timely diagnosis of cervical precancerous lesions are crucial. To identify cervical precancerous lesions, women are referred to colposcopy, which is the most important diagnostic tools to detect cervical precancerous lesions. It allows close visualization of the cervix in order to collect biopsies in the area called transformation zone (TZ), which is where precancerous lesions develop. It is essential for the physician to identify the TZ during colposcopy in order to obtain correct diagnosis. For women aged ≥50 this is often a challenge as TZ naturally with age, will retract further into the cervical canal, making the area for sampling invisible, and thereby the colposcopy inadequate. Consequently, this increases the risk of developing cancer due to diagnostic delay, and the risk of several colposcopy examinations or overtreatment (cone biopsy), before a final diagnosis is achieved. Few studies suggest that pretreatment with local vaginal estrogen prior to colposcopy may improve visualization of the TZ. Thereby, obtaining more accurate biopsies from the cervix, and thus making a more accurate and timely diagnosis in the first outpatient visit. The primary purpose of this study is to evaluate pre-diagnostic treatment with estrogen to improve the diagnosis of women with cervical precancerous lesions, in order to prevent cervical cancer. The study ia s randomized controlled double-blind multicenter study. The investigators will use information from Danish National Patient registry, and data from the Danish Pathology Data Bank. Enrollment will take place at the Departments of Gynecology in Denmark. Eligible women aged ≥ 50 years will be randomized 1:1 to receive local vaginal estrogen or placebo prior to the colposcopic examination. The investigators believe the results will provide the prerequisite for obtaining correct diagnosis, and thereby provide basis for choosing the right individualized examination- and treatment plan. The results will also contribute with important knowledge, that may help reduce the incidence and mortality rate of cervical cancer.
CONDITIONS
Official Title
Improving Diagnostics in Cervical Dysplasia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Postmenopausal women (no bleeding for at least 1 year) aged 50 years or older referred for colposcopy
- Women referred for colposcopy due to a positive HPV test and/or abnormal cervical cytology
- Women referred for colposcopy due to previous abnormal cervical histology with at least 6 months since last colposcopy with biopsies
You will not qualify if you...
- Use of estrogen within the last 3 months in any form
- Previous cervical radiotherapy, cervical amputation, or cone biopsy
- Pregnancy
AI-Screening
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Trial Site Locations
Total: 1 location
1
Department of Gynecology and Obstetrics
Randers, Denmark, 8930
Actively Recruiting
Research Team
V
Vibe M Bertelsen, MD, PhD student
CONTACT
I
Isil Pinar Bor, Ass. professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
2
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