RECRUITING

Usefulness and Feasibility of Ultrasound in Office Laryngology Procedures

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Usefulness and Feasibility of Ultrasound in Office Laryngology Procedures: A Pilot Study

Quick Facts

Study Start:2024-11
Study Completion:2026-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06579989

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * US-Guided Injection for Neurogenic Cough:
  2. 1. Age over 18 years
  3. 2. Recommended to undergo superior laryngeal nerve block
  4. * US-Assessment of Superior Laryngeal Nerve Anatomy
  5. 1. Age over 18 years
  6. 2. No cough complaints
  7. * US-Assessment of Injectate Volume:
  8. 1. Documentation of unilateral vocal fold paresis/paralysis or atrophy
  9. 2. Age over 18 years
  10. 3. Recommended to undergo injection laryngoplasty
  11. * US-Assessment of Swallow:
  12. 1. Age over 18 years
  13. 2. Presents with swallowing complaints
  14. * US-Assessment of Normal Swallow:
  15. 1. Age over 18 years
  16. 2. Presents without swallowing complaints
  17. * US-Assessment of Voice:
  18. 1. Age over 18 years
  19. 2. Undergoing evaluation of voice problems
  1. 1. Age under 18 years and over 99 years
  2. 2. Open neck wound including tracheostomy

Contacts and Locations

Study Contact

Alexandra Li, BS
CONTACT
(646) 962-7464
all4034@med.cornell.edu
Sara Albert, BA
CONTACT
(646) 962-9883
saa4056@med.cornell.edu

Principal Investigator

Anaïs Rameau, MD
PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University

Study Locations (Sites)

Weill Cornell Medicine
New York, New York, 10021
United States

Collaborators and Investigators

Sponsor: Weill Medical College of Cornell University

  • Anaïs Rameau, MD, PRINCIPAL_INVESTIGATOR, Weill Medical College of Cornell University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-11
Study Completion Date2026-06

Study Record Updates

Study Start Date2024-11
Study Completion Date2026-06

Terms related to this study

Additional Relevant MeSH Terms

  • Cough
  • Vocal Cord Atrophy
  • Vocal Cord Paresis
  • Vocal Cord Paralysis
  • Dysphagia
  • Dysphonia