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Clinical Trials/NCT05085093
NCT05085093
Enrolling By Invitation
Not Applicable

Protective Efficacy of HPV Vaccination After Treatment of HPV Related Diseases

Xijing Hospital1 site in 1 country414 target enrollmentSeptember 18, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HPV Vaccination、HPV Related Diseases、Protective Efficacy
Sponsor
Xijing Hospital
Enrollment
414
Locations
1
Primary Endpoint
Persistent HPV infection
Status
Enrolling By Invitation
Last Updated
4 years ago

Overview

Brief Summary

To understand the HPV infection status and subtype distribution of patients, and to study the protective effect of prophylactic HPV vaccination on the recurrence of HPV related diseases after treatment through a prospective cohort study. To provide data support for the primary prevention of HPV related diseases in Chinese women after treatment, and to analyze the related factors of HPV related disease recurrence and HPV continuous positive.

Registry
clinicaltrials.gov
Start Date
September 18, 2021
End Date
September 1, 2024
Last Updated
4 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Xijing Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Women aged 18-45, of childbearing age or before perimenopause (patients without pregnancy plan within two years);
  • Patients diagnosed as condyloma acuminatum, vaginal intraepithelial lesions (high-grade and low-grade lesions), cervical intraepithelial lesions (high-grade and low-grade lesions), vulvar intraepithelial lesions (high-grade and low-grade lesions), cervical cancer (IA1-IIA2 stage) and treated within 3 months;
  • No surgical contraindications such as severe center of heart, lung and other organ dysfunction and abnormal hemagglutination;
  • Fully know the treatment method, sign informed consent, and actively cooperate with follow-up.

Exclusion Criteria

  • Participating in other clinical trials;
  • Use immunoglobulin or blood products within 3 months before vaccination;
  • Hypersensitivity to vaccine active ingredients or any dressing ingredients;
  • Acute stage of moderate and severe diseases;
  • Acute stage of severe immune deficiency diseases and autoimmune diseases;
  • Pregnant women and lactating patients;
  • Patients with planned pregnancy within 2 years;
  • Less than 18 years old and more than 45 years old.

Outcomes

Primary Outcomes

Persistent HPV infection

Time Frame: At least 12 months

At least 12 months apart, cervical vaginal / external genital swabs or tissue biopsies were taken for 2 or more consecutive times, and HPV detection and analysis showed that the same HPV type was positive

recurrence

Time Frame: 6 months after operation

If The lesions were found again more than 6 months after operation (pathological diagnosis)

Study Sites (1)

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