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Rate of high-risk HPV clearance after treatment for cervical cancer

Rate of high-risk HPV clearance after treatment for cervical cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20241026003
Enrollment
270
Registered
2024-10-26
Start date
2025-01-20
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

The current state of uterine cervical cancer reflects both advancements and ongoing challenges. Despite progress in prevention through HPV vaccination and early detection via regular screenings, the disease remains a significant public health concern, especially in low-resource settings. In many regions, limited access to healthcare services, lack of awareness, and delayed diagnosis contribute to higher morbidity and mortality rates. Continued efforts in education, accessible healthcare, and inn

Interventions

A population of 270 participants will be included in the study to monitor the HPV clearance rate at intervals of 3, 6, 12, 18, and 24 months using the Allplex HPV HR detection test. The participants w
Diagnostic
Cervical cancer group

Sponsors

Faculty of Medicine Siriraj Hospital Mahidol University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Female patients diagnosed with cervical cancer receiving treatment at Siriraj Hospital. 2. Age since 18 years. 3. Not pregnant. 4. Able to communicate in Thai. 5. Must have signed a consent form to participate in the research after reading the documents and asking questions about the study until fully understood. 6.Pathological results of all types.

Exclusion criteria

Exclusion criteria: 1. Female patients who have not returned for follow-up examinations after treatment. 2. High-risk HPV has not been detected since the initial diagnosis (non-HPV-related cervical cancer). 3. When a woman declines to participate in the research at any time. 4.Use of zinc sulfate.

Design outcomes

Primary

MeasureTime frame
HPV clearance 0, 3, 6, 12, 18, and 24 months Measurement of HPV DNA less 1-5 copies per cell, mRNA shoud don't have in specimen, and cell-free HPV DNA obtained don't express from blood and swab samples of participant

Secondary

MeasureTime frame
Survival of participant 24 year Monitoring the survival time of participants (Survival follow-up)

Countries

Thailand

Contacts

Public ContactAssoc. Prof. Irene Ruengkhachorn

Gynecologic oncology division of obstetrics and gynecology

irene_siriraj@yahoo.com024194685

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026