Treatment Alternatives in iSGS (NoAAC PR-02 Study)

Trial ID or NCT#

NCT02481817

Status

recruiting iconRECRUITING

Purpose

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?

Official Title

Treatment Alternatives in Adult Rare Disease; Assessment of Options in Idiopathic Subglottic Stenosis North American Airway Collaborative PR-02 Study (NoAAC PR-02 Study)

Eligibility Criteria

Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. - Greater than 18 years of age. - The lesion must involve the subglottis.
Exclusion Criteria:
  1. - 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.
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Investigator(s)

Edward J. Damrose, MD, FACS
Edward J. Damrose, MD, FACS
Laryngologist, Head and neck surgeon, Ear, nose, and throat specialist, Head and neck oncologist
Professor of Otolaryngology - Head & Neck Surgery (OHNS) and, by courtesy, of Anesthesiology, Perioperative & Pain Medicine

Contact us to find out if this trial is right for you.

Contact


650-723-5281

View on ClinicalTrials.gov