Trial Search Results

Treatment Alternatives in iSGS (NoAAC PR-02 Study)

The study is aimed at answering the questions; (1) How well do the most commonly used treatments in iSGS work? and (2) What quality-of-life trade-offs are associated with each approach?

With the results of this trial, the investigators hope to provide information to iSGS patients: (1) Given my personal characteristics, conditions, and preferences, what should I expect will happen to me? and (2) What are my options, and what are the potential benefits and harms of these options?

Stanford is currently accepting patients for this trial.

Lead Sponsor:

Vanderbilt University Medical Center

Collaborator: Patient-Centered Outcomes Research Institute

Stanford Investigator(s):


  • Procedure: Endoscopic dilation of subglottic stenosis
  • Procedure: Endoscopic resection of the stenosis
  • Procedure: Tracheal Resection


Inclusion Criteria:

   - Greater than 18 years of age.

   - The lesion must involve the subglottis.

Exclusion Criteria:

   - Less than 18 years of age

   - Patients without capacity to consent for themselves

   - History of significant laryngotracheal traumatic injury.

   - History of endotracheal intubation or tracheotomy within 2 years of presentation.

   - Major anterior neck surgery.

   - History of neck irradiation.

   - History of caustic or thermal injuries to the laryngotracheal complex.

   - History of a clinically diagnosed vasculitis or collage vascular disease.

   - Positive antinuclear cytoplasmic antibody titers.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study


Now accepting new patients

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305