RecruitingNCT04743674

Blood and Urine HPVDNA as Minimally Invasive Biomarkers for Cervical Cancer Detection and Surveillance Following Treatment

Plasma Circulating Tumor HPVDNA and Transrenal HPVDNA as Minimally Invasive Biomarkers for Cervical Cancer Detection and Surveillance Following Definitive Treatment


Sponsor

UNC Lineberger Comprehensive Cancer Center

Enrollment

30 participants

Start Date

May 3, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this study is to determine if ctHPVDNA (circulating tumor HPV DNA) can be used as a non-invasive biomarker for identification and treatment monitoring of cervical cancer by characterizing correlation between plasma ctHPVDNA, urine transrenal HPVDNA (TrHPVDNA) levels and presence of cervical cancer at diagnosis and following definitive intent management.


Eligibility

Sex: FEMALEMin Age: 18 Years

Inclusion Criteria3

  • years of age or older on day of signing informed consent
  • New diagnosis of cervical cancer
  • Subject is willing and able to comply with study procedures based on the judgement of the investigator or protocol designee

Exclusion Criteria1

  • Women who are pregnant

Locations(2)

Melissa Knutsen

Chapel Hill, North Carolina, United States

Kamuzu Central Hospital

Lilongwe, Malawi

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT04743674


Related Trials