A prospective, multicenter study on the prediction of hr-HPV infection on cervical precancerous lesions via typing and quantitative HPV detection

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000040964

Enrollment

Unknown

Registered

2020-12-16

Start date

2021-01-01

Completion date

Unknown

Last updated

2021-08-30

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

Conditions

premalignant cervical lesion

Interventions

case series:Nil

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: (1) Women aged 25-60 who visited the cervical department and had HPV(+), cytology negative, colposcopy (localized biopsy)/histology negative (women in the status of HPV infection with no lesions); (2) Women with sexual life history; (3) Obtaining informed consent or being able to provide written informed consent.

Exclusion criteria

Exclusion criteria: (1) Women during pregnancy; (2) During the follow-up period, women of childbearing age planned to become pregnant and clearly indicated that they would not accept follow-up after pregnancy; (3) History of cervical surgery: history of hysterectomy or subtotal hysterectomy; (4) Other subjects deemed unfit for inclusion by the investigator.

Design outcomes

Primary

Measure	Time frame
HPV;NILM/LSIL/HSIL;Pathology of colposcopy biopsy;	—

Countries

China

Contacts

Public ContactShujun Gao

Obstetrics and Gynecology Hospital of Fudan University

shujun99@163.com+86 13564819359

Outcome results

None listed

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