Actively Recruiting

Phase 4
Age: 26Years - 65Years
FEMALE
NCT07493824

Single-arm, Prospective Study of the Efficacy and Safety of Paiteling®Antibacterial Liquid in the Treatment of Persistent Cervical HR-HPV Infection

Led by The First Hospital of Jilin University · Updated on 2026-03-25

115

Participants Needed

1

Research Sites

148 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The effectiveness of Patellin ® antibacterial solution in treating persistent cervical HR-HPV infection

CONDITIONS

Official Title

Single-arm, Prospective Study of the Efficacy and Safety of Paiteling®Antibacterial Liquid in the Treatment of Persistent Cervical HR-HPV Infection

Who Can Participate

Age: 26Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 25 to 65 years (inclusive)
  • Persistent cervical HR-HPV infection for at least 2 years with the same high-risk HPV subtype
  • If cervical biopsy is done, it shows chronic cervicitis or low-grade cervical intraepithelial neoplasia
  • Sexual history recorded
  • No anti-HPV treatment (vaginal or systemic) within 3 months before the visit
  • No pregnancy plan within 6 months after the visit
  • Voluntary signing of informed consent
Not Eligible

You will not qualify if you...

  • Cervical biopsy results indicating TCT or high-grade squamous intraepithelial lesion (HSIL)
  • Change or reversal to negative of cervical HR-HPV infection subtype
  • Pregnant or breastfeeding women
  • Acute inflammation of the genital tract
  • Recent immunodeficiency such as chemoradiotherapy, AIDS, or systemic lupus erythematosus
  • Severe diseases including diabetes, cardiovascular, brain, liver, kidney, hematopoietic system disorders, or mental illness
  • History of drug allergy or allergic constitution
  • Participation in other clinical trials within the last 3 months
  • Suspected or confirmed history of alcohol or drug abuse
  • Other conditions reducing enrollment possibility or complicating follow-up (e.g., unstable living or work environment) as judged by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The First Hospital of Jilin University

Changchun, Jilin, China, 130000

Actively Recruiting

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Research Team

X

Xiaosen Li Li

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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