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NCT07203911Recruiting

Surgeon-performed Ultrasound for Real-time Guidance In Oral Cancer Surgeries - A Multicenter Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 13 May 2026

Brief summary (registry, in English)

The goal of this clinical trial is to improve the surgical treatment of patients with oral cancer. We will explore whether the use of surgeon performed ultrasound during these surgeries result in better tumor removal. We hypothesize that using intraoperative ultrasound to assist the resection results in more frequent clear surgical margins in oral cancer surgeries compared to standard methods. This improvement is associated with a reduced need for post-operative adjuvant therapies such as radiotherapy and reoperation, lower mortality rates, lower cancer recurrence, and enhanced quality of life for patients undergoing surgery for oral cancer. Participants will be randomized to either the control or intervention group: * Control group will receive standard treatment for oral cancer. * Intervention group will in addition to the standard treatment have surgery performed using ultrasound to guide the resection and evaluate resection margins intraoperatively. Outcomes: * Number of free surgical margins between control and intervention group. * Intraoperative surgeon assessed surgical margins compared to final histology report. * Dysphagia and quality of life questionnaires. * Recurrence rates. * Mortality rates. All participant will be followed-up at 3 months and 12 months with: * MDADI dysphagia questionnaire * EORTC head and neck cancer quality of life questionnaire * Follow-up on recurrrence and mortality.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
150 (estimated)
First submitted
24 Sept 2025
Start date
15 Sept 2025
Primary completion date
15 Sept 2027
Lead sponsor
Tobias Todsen
NCT number
NCT07203911

What you commit to

  • Study type: Interventional
  • Planned participants: 150
  • From 15 Sept 2025 to the primary completion date, 15 Sept 2027
  • 7 sites in 5 countries
  • 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

  • Prior radiotherapy treatment of oral cavity cancer.

Other illness

  • Oral cancer with suspected bone involvement.

Age

  • Age \< 18 years.

Other

  • Unable to understand verbal or written information.
  • Tumor not visible on ultrasound.

Who the study is looking for

  • Patients scheduled for surgical treatment of biopsy-proven T1-T3 oral squamous cell carcinoma.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

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

SiteCityCountrySite status
Department of Otorhinolaryngology Head and Neck Surgery
Coordinator of this site? Confirm its status
AarhusDenmarkRecruiting
Department of Otorhinolaryngology Head and Neck Surgery and Audiology, Rigshospitalet
Coordinator of this site? Confirm its status
CopenhagenDenmarkRecruiting
Istituto Nazionale Tumori of Milan
Coordinator of this site? Confirm its status
MilanItalyNot yet recruiting
Karolinska Institute
Coordinator of this site? Confirm its status
StockholmSwedenRecruiting
Emory University Hospital
Coordinator of this site? Confirm its status
AtlantaUnited StatesNot yet recruiting
Stanford Otolaryngology - Head & Neck Surgery Department
Coordinator of this site? Confirm its status
StanfordUnited StatesNot yet recruiting
Groote Schuur
Coordinator of this site? Confirm its status
Cape TownSouth AfricaNot yet recruiting

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