Human Papillomavirus Infection Clinical Trials

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Dynamic Monitoring of Circulating Tumor DNA (ctDNA) and HPV DNA in Plasma for the Early Prediction of Recurrence After Cervical Cancer Surgery/Treatment

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

Assess the sensitivity, specificity, positive predictive value, and negative predictive value of dynamic monitoring of circulating tumor DNA (ctDNA) combined with circulating HPV DNA (cfHPV DNA) for early prediction of recurrence in cervical cancer post-surgery or post-treatment, and compare its advantages and disadvantages with existing diagnostic methods.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with newly diagnosed HPV-positive cervical malignancy at stages I-IV who have not undergone surgery, radiation therapy, or chemotherapy.

• Patients must be older than 18 years of age.

• Cervical cancer patients who are eligible for surgery and/or chemoradiotherapy.

• Estimated life expectancy of more than three months.

• Understands the study protocol and voluntarily participates in the research by signing the informed consent form.

• Able to provide specimens and corresponding clinical information at each time point.

Locations
Other Locations
China
The Third Affiliated Hospital of Guangzhou Medical University
RECRUITING
Guangzhou
Contact Information
Primary
Xiujie Sheng, Prof
2008691150@gzhmu.edu.cn
86-20-81292726
Time Frame
Start Date: 2024-01-01
Estimated Completion Date: 2027-01-30
Participants
Target number of participants: 150
Sponsors
Leads: The Third Affiliated Hospital of Guangzhou Medical University

This content was sourced from clinicaltrials.gov