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The Predictive Role of HPV Integration in HSIL and Cervical Cancer

The Predictive Role of HPV Integration in HSIL and Cervical Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05300243
Enrollment
1
Registered
2022-03-29
Start date
2020-07-07
Completion date
2022-06-01
Last updated
2022-03-29

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

Conditions

HPV Integration

Brief summary

The stratified analysis by the level of HPV DNA integration in HSIL and cervical cancer will be drawn to explore whether the status of HPV integration makes any difference in the progression of cervical cancer. The purpose of the research is to reduce the miss of cervix lesions and prove that HPV integration detection is sensitive in cervical cancer precise screening.

Interventions

DIAGNOSTIC_TESTHPV integration test

The stratified analysis by the level of HPV DNA integration in HSIL and cervical cancer will be drawn to explore whether the status of HPV integration makes any difference in the progression of cervical cancer. The purpose of the research is to reduce the miss of cervix lesions and prove that HPV integration detection is sensitive in cervical cancer precise screening.

Sponsors

Tongji Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* HPV-positive patients; Patients have completed HPV detection, TCT, and HPV integration detection before surgery or biopsy; Patients with priced diagnoses accepted treatment according to ASCCP Risk-Based Management Consensus Guidelines for Abnormal Cervical Cancer Screening Tests and Cancer Precursors; Patients who are voluntary participants in this research and cooperate to follow-up with subscribing informed consent.

Exclusion criteria

* Patients who are not suitable for the trial; Patients existing other subtype malignancy tumors are still in treatment.

Design outcomes

Primary

MeasureTime frameDescription
Tissue pathological diagnosis1year since HPV integrated testTissue pathological diagnosis in 1 year since HPV integrated test

Countries

China

Contacts

Primary ContactShuang Li, PHD
shuangli@hust.edu.cn+86 18971625668

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026