Status:

NOT_YET_RECRUITING

Assessment of Laryngopharyngeal Sensation: Cancer Survivor Cohort

Lead Sponsor:

University of California, San Francisco

Collaborating Sponsors:

National Spasmodic Dysphonia Association

Conditions:

Presbylarynx

Aspiration

Eligibility:

All Genders

18-85 years

Phase:

NA

Brief Summary

A previous study completed in 2022 (NCT05158179) was conducted using cohorts of healthy controls, and adults with general laryngopharyngeal disorders. This study will expand on the previous research t...

Detailed Description

PRIMARY OBJECTIVES: I. Laryngeal sensation as measured by elicitation of laryngeal adductor reflex (LAR). II. To compare the elicitation of laryngeal adductor reflex (LAR) threshold/probability to t...

Eligibility Criteria

Inclusion

  • Age \<=18 years.
  • Individuals without a laryngopharyngeal disorder (health controls) or with a laryngopharyngeal disorder. Laryngopharyngeal disorder includes but is not limited to: presbylarynx, aspiration; spasmodic dysphonia; globus pharynges; vocal fold paralysis; iatrogenic injury to the larynx; muscle tension dysphonia; neurogenic dysphagia; laryngeal sensory neuropathy; and laryngopharyngeal disorders resulting from prior radiation therapy in individuals with a history of head and neck cancer who have completed radiation therapy as primary or adjuvant cancer treatment
  • Ability and willingness to comply with study procedures.
  • Ability to understand a written informed consent document, and the willingness to sign it.

Exclusion

  • Non-English speaking.
  • Laryngopharyngeal structures are not accessible on exam.
  • Known contraindication to any study-related procedure, or history of being unable to tolerate laryngoscopy.
  • Vocal fold immobility or severe hypomobility on adduction.
  • For head and neck cancer survivors only: Currently undergoing radiation therapy for head and neck cancer (i.e., primary/adjuvant radiation therapy treatment plan is not yet completed).

Key Trial Info

Start Date :

October 1 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

January 31 2028

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT06078527

Start Date

October 1 2025

End Date

January 31 2028

Last Update

July 23 2025

Active Locations (1)

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1

University of California, San Francisco

San Francisco, California, United States, 94143