Blood and Urine HPVDNA as Minimally Invasive Biomarkers for Cervical Cancer Detection and Surveillance Following Treatment
Recruiting now
Conditions studied: Cervical Cancer
In brief
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.
Key facts
- Study ID
- NCT04743674
- Run by
- UNC Lineberger Comprehensive Cancer Center
- People needed
- 30
- Starts
- 2024-05-03
- Expected to finish
- 2027-01-15
- Last updated by the study team
- 2026-05-12
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- 18 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
You may not qualify if…
- Women who are pregnant
Where it is running
- Melissa Knutsen — Chapel Hill, North Carolina, United States (enrolling)
- Kamuzu Central Hospital — Lilongwe, Malawi
Full record on ClinicalTrials.gov
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