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NCT04274465Completed

Application of Plasma Circulating HPV DNA Testing to Management of Cervical Intraepithelial Neoplasia

Application of Plasma Circulating Human Papillomavirus (HPV) DNA Testing to Management of Cervical Intraepithelial Neoplasia

Source: ClinicalTrials.gov · Last updated 14 Nov 2024

Brief summary (registry, in English)

The purpose of this study is to see if circulating HPV DNA (cHPVDNA) can be used as a noninvasive biomarker for cervical intraepithelial neoplasia (CIN) 2-3 in hopes of reducing procedures and costs for patients, as well as personalize their treatment plan.

Status (registry)
Completed
Study type
Observational
Enrollment
145 (actual)
First submitted
14 Feb 2020
Start date
26 Feb 2020
Primary completion date
26 Jun 2024
Lead sponsor
UNC Lineberger Comprehensive Cancer Center
NCT number
NCT04274465

What you commit to

  • Study type: Observational
  • Participants enrolled: 145
  • From 26 Feb 2020 to the primary completion date, 26 Jun 2024
  • 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.

Other

  • Women who are pregnant or nursing

Who the study is looking for

  • No history of previously treated cervical cancer
  • Subject is willing and able to comply with study procedures based on the judgement of the investigator or protocol designee

Age in the registry: 18 years to 99 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tuvara Jenene King
Coordinator of this site? Confirm its status
Chapel HillUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.