Effect of HPV Integration on Prognosis of Young Women With CIN2 in China
Recruiting
Observational Study
Cervical Intraepithelial Neoplasia
HPV Infection
Virus Integration
HSIL, High Grade Squamous Intraepithelial Lesions
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- Up to 45
- Sex
- Female
- Study type
- Observational
- Participants needed
- 300 (estimated)
- Sponsor
- Fujian Maternity and Child Health Hospital · Other
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About This Trial
Clinically, cervical precancerous lesion is one of the important diseases that endanger the life safety and fertility of young women. Women with histopathologically confirmed CIN2 need regular HPV, cervical cytology, and colposcopic biopsy if necessary to assess the outcome and progression of the disease. In this study, we intend to visit Fujian Maternal and Child Health Hospital, Tongji Hospital …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Female, 18 years of age or older and 45 years of age or younger, with a desire to conceive;
* Diagnosed with HSIL (CIN2) or HSIL (CIN2-3) via cervical tissue biopsy within the past 3 months, and has not undergone cervical surgery, physical, or medication treatment;
* The lesio…
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