Actively Recruiting

Age: 18Years +
All Genders
NCT05665244

Laryngeal Cryotherapy for Refractory Neurogenic Cough

Led by University of Texas Southwestern Medical Center · Updated on 2026-01-30

28

Participants Needed

1

Research Sites

214 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the safety and efficacy of upper aerodigestive tract cryotherapy treatment in patients with refractory neurogenic cough in a prospective pilot study with a validated patient reported outcome measure

CONDITIONS

Official Title

Laryngeal Cryotherapy for Refractory Neurogenic Cough

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients 18 years or older with diagnosis of neurogenic cough
  • Neurogenic cough diagnosed after excluding other causes with persistent cough lasting 8 weeks or longer
  • Negative evaluation for sinonasal allergies, chronic sinusitis, cough-variant asthma, and GERD
  • Willingness to participate in a clinical trial
Not Eligible

You will not qualify if you...

  • Uncontrolled reflux with a Reflux Symptom Index score of 13 or higher
  • Vocal fold abnormalities or impairment
  • History of asthma or lung conditions that are not well controlled
  • Uncontrolled allergic rhinitis with Total Nasal Symptom Score greater than 6
  • Symptoms of postnasal drip
  • Current smoking
  • Use of neuromodulator medications
  • Unwillingness to participate or sign informed consent
  • End stage medical disease with poor life expectancy
  • Medical instability preventing enrollment
  • Abnormal chest X-ray results
  • Abnormal pulmonary function tests
  • Positive local allergy panel (combined RAST testing)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UT Southwestern Medical Center

Dallas, Texas, United States, 75235

Actively Recruiting

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Research Team

S

Shumon Dhar, MD

CONTACT

P

Paula Arellano-Cruz

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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