Fact CheckerSign in

NCT05919290Recruiting

HN-QUEST: A Study of Head and Neck Imaging Biomarkers

HN QUEST- Evaluation of Online MRgRT and Repeat Functional Imaging in Patients Undergoing Curative (CT)RT for HN Malignancy

Source: ClinicalTrials.gov · Last updated 5 Mar 2026

Brief summary (registry, in English)

This is a multi arm, single center, investigator initiated study to investigate online adaptive radiotherapy and biomarker development in patients with newly diagnosed HNSCC (Head and Neck Squamous Cell Carcinoma) receiving curative therapy. The study will consist of two prospective arms. In Arm 1 up to 100 HNSCC patients receiving (CT)RT (computed tomography-based radiation therapy) will receive up to weekly non-contrast MRI (magnetic resonance imaging) scans during treatment. Arm 2 consists of two cohorts. In cohort A up to 20 healthy volunteers will undergo non-contrast MRI at two time points. In cohort B up to 53 patients planned to receive curative (chemo) radiotherapy for HNSCC will undergo two baseline MRI scans, one MRI in week 2 and week 4, and final MRI scan 6-8 weeks after completion of treatment.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
173 (estimated)
First submitted
8 Jan 2023
Start date
26 Jul 2023
Primary completion date
1 Jul 2029
Lead sponsor
University Health Network, Toronto
NCT number
NCT05919290

What you commit to

  • Study type: Interventional
  • Planned participants: 173
  • From 26 Jul 2023 to the primary completion date, 1 Jul 2029
  • 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

  • Previous solid tumor treated within last 5 years

Other illness

  • As judged by investigator evidence of systemic disease that makes unsuitable for study
  • History of significant obstructive airway disease
  • History of gadolinium contrast allergy
  • Underlying significant respiratory disease

Other

  • Contra-indication for serial MRI scans
  • Pregnancy
  • Unwillingness to sign informed consent
  • Contra-indication for MRI

Who the study is looking for

  • Age \>/= 18 years
  • Histologically proven Head and Neck Squamous Cell carcinoma
  • Primary or nodal disease \> 3cm for biomarker imaging
  • Eastern Cooperative Oncology Group (ECOG) Performance Status 0-2
  • Planned for curative surgery or (chemo)radiotherapy
  • Willingness to undergo repeat MRI
  • Able to receive and understand verbal and written information regarding study and able to give written informed consent
  • Adequate renal function: Calculated creatinine clearance \>/= 30ml/min
  • Be able to lie comfortably on back for 1 hour
  • Age \>/= 18 years
  • Able to receive and understand verbal and written information regarding study and able to give written informed consent
  • Willingness to undergo repeat MRI

Age in the registry: 18 years to - · Sex: All · 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
Princess Margaret Cancer Centre
Coordinator of this site? Confirm its status
TorontoCanadaRecruiting

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