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NCT04599309Active, not recruiting

Real-time Detection of ctDNA and/or HPV DNA in High-risk Locally-advanced Head and Neck Squamous Cell Carcinoma

Real-time Detection of ctDNA and/or HPV DNA in High-risk Locally-advanced Head and Neck Squamous Cell Carcinoma (LA-HNSCC): The Pre-MERIDIAN (Molecular Residual Disease Interception in High-risk LA-HNSCC) Study.

Source: ClinicalTrials.gov · Last updated 10 Jun 2026

Brief summary (registry, in English)

This research study will include patients with high risk locally advanced head and neck squamous cell carcinoma (LA-HNSCC) of the oral cavity, oropharynx, hypopharynx or larynx and patients that are starting on standard definitive treatment. Patients with both stage III HPV positive and stage III HPV negative will be included. In this study, we aim to evaluate feasibility of ctDNA and/or HPV DNA detection in real time in high-risk LA-HNSCC.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
35 (actual)
First submitted
18 Oct 2020
Start date
15 Oct 2020
Primary completion date
31 Mar 2023
Lead sponsor
University Health Network, Toronto
NCT number
NCT04599309

What you commit to

  • Study type: Observational
  • Participants enrolled: 35
  • From 15 Oct 2020 to the primary completion date, 31 Mar 2023
  • 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

  • Early stage HNSCC (I and II)
  • Distant metastatic HNSCC

Who the study is looking for

  • Histologically or cytological confirmed LA-HNSCC of the oral cavity, oropharynx, hypopharynx, or larynx.
  • Stage III HPV Positive or Stage III-IV HPV negative.
  • Availability of tumor sample
  • Patients who are candidates for standard definitive treatment defined as:
  • Surgery followed by radiotherapy +/- chemotherapy OR
  • Definite radiotherapy OR
  • Definite chemoradiotherapy.

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
Princess Margaret Cancer Centre
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status

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