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Completed

NCT Number: NCT02481817

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?

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Sydney, St Leonards, Australia

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About this study

Idiopathic subglottic stenosis (iSGS) is a rare disease in which the trachea narrows for no known reason. Although uncommon (with an estimated incidence of 1:400,000 persons per year), both the disease and its therapies profoundly affect patients' ability to breathe, communicate and swallow. Breathing difficulties (i.e. dyspnea) is the hallmark symptom and the primary cause of death and disability. However, patients can also experience debilitating voice changes and swallowing problems due to the condition or its treatment.

People with this disease often require several surgeries per year. A variety of treatments have been advanced to manage iSGS but are generally categorized into: 1) endoscopic dilation of the tracheal stenosis (accomplished with rigid instruments or inflatable balloons); 2) endoscopic resection of the stenosis (with prolonged medical therapy after surgery); or 3) open neck surgery with resection of the affected tracheal segment with end-to-end anastomosis. Each patient can require repeated surgeries to keep their trachea open, which increases odds of treatment side effects and complications. All approaches have unique and often disabling associated side effects, which can significantly affect a patient's quality of life.

Because the disease is rare, it is difficult for patients to find good information so that they can understand the spectrum of treatment options. This is particularly difficult because most patients present with severe breathing trouble and need treatment quickly, limiting their ability to explore options. Additionally, there is a general lack of high-quality, reliable, and accessible data to inform individual patient decision-making. Imperfect information and limited evidence on treatment outcomes complicate patient decision-making as they try to balance survival, symptoms, and quality of life considerations.

Beyond the gaps in understanding the relative effectiveness of the different treatments available, no studies have explored functional outcomes in iSGS (i.e. how well patients breathe, speak, and swallow after treatments). These endpoints are important to patients and are arguably a primary determinant in decision-making. Direct engagement with patients is critical to understand these quality of life considerations, since patient and physician perspectives aren't always the same. For example, results show that endoscopic dilation is associated with a higher rate of disease recurrence and thus need for repeated surgery. Meanwhile, open tracheal resection is a major surgery with significant immediate perioperative risks and has been associated with alterations in voice and swallowing. Open tracheal resection appears to reduce the risk of disease recurrence, but the degree of benefit, and the trade-offs associated with this approach are unanswered questions.

The proposed study from the North American Airway Collaborative (NoAAC PR- 02) is designed to fill this void. Our prospective study will directly compare the effectiveness of standard of care treatments and assess their associated quality of life tradeoffs in iSGS patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Endoscopic dilation of subglottic stenosis

Procedure

This is accomplished with rigid instruments or inflatable balloons.

Endoscopic resection of the stenosis

Procedure

This is accomplished with C02 lasers and paired with prolonged medical therapy after surgery.

Tracheal Resection

Procedure

Resection of the affected tracheal segment with end-to-end anastomosis

Other names: Cricotracheal Resection, Open Airway Surgery

Primary outcomes

  1. Treatment Effectiveness: Time to recurrent procedure

    Time frame: 3 years

  2. Treatment Effectiveness: Need for tracheostomy

    Time frame: 3 years

Secondary outcomes

  1. QOL

    Time frame: 3 years

    Patient quality of life assessment: voice (VHI-10)

  2. QOL

    Time frame: 3 years

    Patient quality of life assessment: dysphagia (EAT-10)

  3. QOL

    Time frame: 3 years

    Patient quality of life assessment: breathing (COPD dyspnea)

  4. QOL

    Time frame: 3 years

    Patient quality of life assessment: general quality of life (SF-12)

  5. Patient Reported Outcome

    Time frame: 3 years

    Non-traditional PRO focused on social support

  6. Patient Reported Outcome

    Time frame: 3 years

    Non-traditional PRO focused on fear of disease recurrence

  7. Patient Reported Outcome

    Time frame: 3 years

    Non-traditional PRO focused on disease anxiety and burden

  8. Patient Reported Outcome

    Time frame: 3 years

    Non-traditional PRO focused on participatory decision-making style

Sponsors and collaborators

Lead sponsor

Vanderbilt University Medical Center

Other

Collaborators

  • Augusta University
  • Bastian Voice Institute
  • Baylor College of Medicine
  • Charing Cross Hospital
  • Duke University
  • Emory University
  • Johns Hopkins University
  • Landspitali University Hospital
  • Loma Linda University
  • Louisiana State University Health Sciences Center in New Orleans
  • Massachusetts Eye and Ear Infirmary
  • Mayo Clinic
  • Medical College of Wisconsin
  • NYU Langone Health
  • North American Airway Collaborative
  • Ohio State University
  • Oregon Health and Science University
  • Patient-Centered Outcomes Research Institute
  • Stanford University
  • Temple University
  • The Cleveland Clinic
  • University of Alabama at Birmingham
  • University of California, Irvine
  • University of California, Los Angeles
  • University of California, San Diego
  • University of California, San Francisco
  • University of Cincinnati
  • University of Colorado, Denver
  • University of Iowa
  • University of Miami
  • University of Michigan
  • University of Nebraska
  • University of North Carolina
  • University of Pittsburgh
  • University of Rochester
  • University of Southern California
  • University of Sydney
  • University of Texas
  • University of Utah
  • University of Virginia
  • University of Washington
  • University of Wisconsin, Madison
  • Vanderbilt University

Registry information

Official study 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)

Acronym: NoAAC PR-02

Important dates

Study start
2015
Primary completion
2020
Study completion
2020
First posted
Jun 25, 2015
Registry last updated
Oct 28, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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