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NCT06730412Completed

ctDNA Liquid Biopsy for Early Assessment of Residual Disease in HPV-associated Head and Neck Cancer (Clear-HPVca)

Source: ClinicalTrials.gov · Last updated 4 Dec 2025

Brief summary (registry, in English)

The purpose of this study is to test a new liquid biopsy assay for detecting residual disease after surgery in patients with HPV-associated head and neck cancer.

Status (registry)
Completed
Study type
Observational
Enrollment
103 (actual)
First submitted
9 Dec 2024
Start date
1 Aug 2020
Primary completion date
31 Oct 2024
Lead sponsor
Massachusetts Eye and Ear Infirmary
NCT number
NCT06730412

What you commit to

  • Study type: Observational
  • Participants enrolled: 103
  • From 1 Aug 2020 to the primary completion date, 31 Oct 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.

Prior treatment

  • Receiving treatment for concurrent second malignancy

Other

  • Not meeting all inclusion criteria
  • Pregnant

Who the study is looking for

  • Greater than or equal to 18 years of age
  • Newly diagnosed, untreated, histologically confirmed HPV-associated head and neck cancer
  • Scheduled for curative intent resection as primary treatment
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-2

Age in the registry: 18 years to - · Sex: All · Does not accept 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
Department of Otolaryngology - Head and Neck Surgery, Massachusetts Eye and Ear Infirmary
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

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