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Recruiting NCT07434583

NCT07434583 Force Sensor Study

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Clinical Trial Summary
NCT ID NCT07434583
Status Recruiting
Phase —
Sponsor University of California, San Francisco
Condition Laryngeal Disease
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2026-01-02
Primary Completion 2027-01-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Direct laryngoscopy force modulationDirect laryngoscopy without force modulation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 100 participants in total. It began in 2026-01-02 with a primary completion date of 2027-01-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This research is to understand more about the forces that are involved on the tongue and other oropharyngeal structures during laryngeal surgery. This information will be used to determine if these forces can affect outcomes (pain, numbness, taste, etc) and whether factors such as procedure type, surgeon experience (i.e. resident, fellow, attending), and choice of surgical equipment affect these forces. This information may be used to reduce these forces and prevent these issues from happening during certain laryngeal surgeries. For the first 50 patients, force measurements will be taken and correlated to outcome measures . Surgeons will be blinded to the force measurements intra-operatively. For the next 50 patients, surgeons will be given force measurements in real-time intra-operatively allowing adjustments to be made. The impact of this adjustment on outcomes will be determined.

Eligibility Criteria

Inclusion Criteria: * \>18 years old with * undergoing laryngeal surgery with direct laryngoscopy Exclusion Criteria: * Prior history of tongue dysfunction such as glossectomy (hemi or total) or hypoglossal nerve injury * Patient inability to follow up after initial procedure

Contact & Investigator

Central Contact

Riley Jackson

✉ riley.jackson@ucsf.edu

📞 6282526882

Principal Investigator

Tyler Crosby, MD

PRINCIPAL INVESTIGATOR

University of California, San Francisco

Frequently Asked Questions

Who can join the NCT07434583 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Laryngeal Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07434583 currently recruiting?

Yes, NCT07434583 is actively recruiting participants. Contact the research team at riley.jackson@ucsf.edu for enrollment information.

Where is the NCT07434583 trial being conducted?

This trial is being conducted at San Francisco, United States.

Who is sponsoring the NCT07434583 clinical trial?

NCT07434583 is sponsored by University of California, San Francisco. The principal investigator is Tyler Crosby, MD at University of California, San Francisco. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology