Vocal Cord Paralysis

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Review clinical trials related to Vocal Cord Paralysis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Usefulness and Feasibility of Ultrasound in Office Laryngology Procedures

Investigators will assess the usefulness of using ultrasound in office procedures for laryngology interventions. Participants who qualify will be adults who are undergoing superior laryngeal nerve block, injection laryngoplasty, swallowing evaluation, voice evaluation and voice therapy.

Participants needed: 200
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: Weill Medical College of Cornell UniversityUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Age over 18 years [+13]

Age under 18 years and over 99 years [+1]

Status: Recruiting

Detection of Vocal Fold Motion Impairment on Noninvasive Positive Pressure

The goal of this prospective, observational study is to evaluate for the presence of vocal fold motion impairment (VFMI) in the children admitted to the pediatric intensive care unit on noninvasive positive pressure ventilation (NIV PPV). Participants will have two ultrasounds of their vocal folds performed, once while on NIV PPV and once after weaned off of the NIV PPV. This results of these scans will be reviewed against one another and against the gold standard, fiberoptic nasolaryngoscopy (FNL). The main question this study aims to answer is: Can POCUS be used to reliably detect VFMI while pediatric patients on supported with NIV PPV?

Participants needed: 50
Trial details
Age: 1-18Biological sex: AllType: ObservationalSponsor: Nemours Children's ClinicUpdated: May 6, 2026Locations: 1
Eligibility criteria

Age 0 to 18 years [+2]

Tracheostomy in place [+3]

Status: Not yet recruiting

Assessment of Laryngopharyngeal Sensation: Cancer Survivor Cohort

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 to include a separate cohort of adults being seen in clinic for an existing laryngopharyngeal disorder resulting from previous radiation or other cancer treatments.

Participants needed: 40
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: University of California, San FranciscoUpdated: Jul 23, 2025Locations: 1
Eligibility criteria

Age <=18 years. [+3]

Non-English speaking. [+4]