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A prospective cohort study on the natural outcome of persistent HPV positive in women in northeastern Sichuan and the efficacy of different intervention methods

A prospective cohort study on the natural outcome of persistent HPV positive in women in northeastern Sichuan and the efficacy of different intervention methods

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059632
Enrollment
Unknown
Registered
2022-05-05
Start date
2022-05-04
Completion date
Unknown
Last updated
2024-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HPV

Interventions

observation group:no intervention
therapy group1:HIFU treatment
therapy group2:Interferon treatment

Sponsors

Nanchong central hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Have no history of cervical surgery and complete uterus; 2. Women with persistent HPV positive (two consecutive HPV positive cases in 6 months); 3. No other diseases; 4. Not pregnant and without suspected pregnancy symptoms; 5. Have a history of sexual life; 6. At present, there is no evidence of cervical lesions in the cervical examination.

Exclusion criteria

Exclusion criteria: 1. Currently in pregnancy or within three months after termination of pregnancy; 2. Not willing to participate in the project.

Design outcomes

Primary

MeasureTime frame
Postoperative HPV clearance rate;HPV natural clearance rate;—

Secondary

MeasureTime frame
Colposcopy;HPV DNA test;LSIL/HSIL;—

Countries

China

Contacts

Public ContactXu Fan
xufanyidingxin@163.com+86 15984877283

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026