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Not Yet RecruitingNCT07074392

Assessing Spinal Accessory Nerve Recovery After Post-operative Electrical Stimulation

Assessing the Feasibility and Effect of Post-operative Electrical Stimulation on Spinal Accessory Nerve Recovery After Neck Dissection for Head and Neck Cancer

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
38 (estimated)
Sponsor
McMaster University · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Shoulder weakness and pain are common after neck dissection surgery for head and neck cancer. This is often caused by injury to the spinal accessory nerve, which controls important shoulder muscles. Recovery can be slow and incomplete, affecting patients' ability to return to daily activities. This project will test whether a brief, low-dose electrical stimulation treatment can help the nerve heal faster and improve shoulder function. The treatment is applied during surgery and is safe, non-invasive, and quick to deliver. If successful, this approach could lead to better rehabilitation, less disability, and improved quality of life for patients undergoing cancer surgery. The project also supports the development of new medical technology and offers a pathway to expand the use of electrical stimulation in other nerve injuries.

Conditions

Interventions

TypeNameDescription
DEVICEElectrical StimulationCustom stimulator will deliver a 1hour stimulation protocol post-operatively at 20 Hz, with biphasic pulses (100 µs duration, 0-2mA amplitude range).

Timeline

Start date
2026-01-01
Primary completion
2027-01-01
Completion
2027-03-01
First posted
2025-07-20
Last updated
2025-08-19

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT07074392. Inclusion in this directory is not an endorsement.

Assessing Spinal Accessory Nerve Recovery After Post-operative Electrical Stimulation (NCT07074392) · Clinical Trials Directory