Early swallowing and speech intervention for head and neck cancer patients after surgery
Official title: Feasibility of Early Swallowing and Speech Intervention for Head and Neck Cancer Patients Treated SURGically
Run by University Health Network, Toronto · NCT06192771 · Data updated 2026-11-12
This study is testing if early help from speech therapists can improve swallowing and speech for patients with tongue cancer after surgery to prevent complications.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | University Health Network, Toronto Academic / other |
| Locations | 1 site (Toronto, Ontario) |
| Status | Recruiting |
| Started | December 1, 2023 |
| Main results expected | December 31, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | June 3, 2026 |
| Trial ID | NCT06192771 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are newly diagnosed patients with at least T2 stage tongue squamous cell carcinoma scheduled for partial glossectomy.
✕Probably not a fit
Patients planned for total glossectomy will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the feasibility of early intervention by speech-language pathologists for patients with head and neck cancer who are undergoing surgery. It focuses on newly diagnosed patients with tongue squamous cell carcinoma who will have partial glossectomy and aims to implement swallow strategies before complications arise. The goal is to improve patient health and function, potentially reducing the risk of dysphagia-related complications and the need for feeding tubes. The study will assess the practicality of conducting a larger clinical trial based on these interventions.
Why it matters
Potential benefit: If successful, this approach could significantly improve the quality of life for head and neck cancer patients by reducing swallowing difficulties and associated complications.
How similar studies have gone: Emerging evidence suggests that early intervention strategies in similar contexts have shown promise, indicating potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Newly diagnosed patients with at least T2 stage tongue SCC who are planned for partial glossectomy and free flap reconstruction and are anticipated to achieve a post-operative independent oral intake. * Proficient in spoken and written English Exclusion Criteria: * Patients who are planned for total glossectomy
Where it's running
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University Health Network
Toronto, Ontario, Canada Recruiting
Study contacts
- Principal investigator: Rosemary Martino, PhD — University Health Network, Toronto
- Study coordinator: Trixie Reichardt, MHSc
- Email: trixie.reichardt@uhnresearch.ca
- Phone: 416-946-3826
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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This pilot test sees if tailoring pain treatment to a patient’s pain type can reduce head and neck cancer pain in adults who haven’t started cancer treatment yet.
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Iparomlimab and Tuvonralimab With Cetuximab Before Surgery in Resectable Oral Cancer
In this phase 2 study, patients with locally advanced, resectable oral squamous cell carcinoma will receive a combination of iparomlimab, tuvonralimab, and cetuximab before surgery to see if the treatment is safe and can shrink tumors.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.