NCT07777094Active, not recruiting
TS Triage of HR-HPV Positive Population and Its Accuracy Study
A Study on the Application of TS for Triage in HR-HPV Viral Load Positive Population and Accuracy Related Studies
Source: ClinicalTrials.gov · Last updated 20 Aug 2026
Brief summary (registry, in English)
A prospective study assessing TS accuracy in HR-HPV+ women, influencing factors, and 1-year follow-up of false-positives versus biopsy.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 300 (estimated)
- First submitted
- 17 Aug 2026
- Start date
- 1 Oct 2024
- Primary completion date
- 31 Dec 2027
- Lead sponsor
- Affiliated Hospital of Nantong University
- Diseases
- Cervical cancer, Childhood cancers
- NCT number
- NCT07777094
What you commit to
- Study type: Observational
- Planned participants: 300
- From 1 Oct 2024 to the primary completion date, 31 Dec 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Within three months after cervical surgery (including cervical biopsy);
- Previous radiotherapy in the pelvic region;
- Currently undergoing chemotherapy or within five weeks after chemotherapy;
Other illness
- Clinically evident acute or subacute cervical/vaginal infection;
- History of photosensitivity disorders, current photodynamic therapy, or exposure to photosensitizing agents;
- Suspected or confirmed history of alcohol/drug abuse, or any other condition that-in the investigator's judgment-may reduce enrollment feasibility or complicate participation (e.g., frequent job relocation, unstable living conditions leading to high risk of loss to follow-up);
Other
- Patients who are unable to cooperate or have poor compliance;
- Within four months postpartum;
- During the first three days of menstruation with heavy flow;
- Other patients deemed ineligible by the investigators.
Who the study is looking for
- Patients in our outpatient clinic who have already undergone HPV viral load testing and are awaiting colposcopy, or those who have both HPV viral load test results and TS (Triple Staining) results and are awaiting colposcopy；
- Informed consent obtained from voluntary participants.
Sex: Female · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Affiliated Hospital of Nantong University Coordinator of this site? Confirm its status | Nantong | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.