Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07434583

Biomechanical Analysis of Force Loadings During Suspension Microlaryngoscopy

Led by University of California, San Francisco · Updated on 2026-02-25

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the forces on the tongue and nearby structures during laryngeal surgery to understand how these forces might affect patient outcomes like pain, numbness, and taste changes. The study also looks at whether factors such as the type of procedure, surgeon experience, and surgical tools influence these forces. This information aims to help reduce harmful forces and improve surgical results. The study involves two groups of patients undergoing direct laryngoscopy. For the first 50 patients, force measurements will be taken during surgery but surgeons will not see them. For the next 50 patients, surgeons will receive real-time force data during surgery and can adjust their technique to reduce force. Post-operative outcomes will be collected in both groups. Participants will have assessments including pain questionnaires at 1 day, 14 days, and 1 month after surgery. Researchers will also evaluate tongue movement, sensation, and taste changes during follow-up visits. The study is planned to run until early 2027 and is sponsored by the University of California, San Francisco.

CONDITIONS

Brief Title

Force Sensor Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Undergoing laryngeal surgery with direct laryngoscopy
Not Eligible

You will not qualify if you...

  • Prior history of tongue dysfunction such as hemi or total glossectomy or hypoglossal nerve injury
  • Inability to attend follow-up visits after the initial procedure

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Day of surgery

Participants undergo direct laryngoscopy with or without force modulation during surgery, followed by immediate post-operative care where force measurements are taken intra-operatively.

1 visit (in-person)

Post-operative Follow-up

Duration - Up to 1 month post-operatively

Participants attend follow-up visits to assess pain, tongue mobility, sensation, and taste changes after surgery.

3 visits (1 day, 14 days, and 1 month post-operatively)

Trial Site Locations

Total: 1 location

1

University of California San Francisco

San Francisco, California, United States, 94115

Actively Recruiting

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Research Team

R

Riley Jackson

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

FACTORIAL

Primary Purpose

PREVENTION

Number of Arms

2

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