Endoscopic dilation of subglottic stenosis
ProcedureThis is accomplished with rigid instruments or inflatable balloons.
NCT Number: NCT02481817
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?
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
University of Sydney, St Leonards, Australia
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
This is accomplished with rigid instruments or inflatable balloons.
This is accomplished with C02 lasers and paired with prolonged medical therapy after surgery.
Resection of the affected tracheal segment with end-to-end anastomosis
Other names: Cricotracheal Resection, Open Airway Surgery
Time frame: 3 years
Time frame: 3 years
Time frame: 3 years
Patient quality of life assessment: voice (VHI-10)
Time frame: 3 years
Patient quality of life assessment: dysphagia (EAT-10)
Time frame: 3 years
Patient quality of life assessment: breathing (COPD dyspnea)
Time frame: 3 years
Patient quality of life assessment: general quality of life (SF-12)
Time frame: 3 years
Non-traditional PRO focused on social support
Time frame: 3 years
Non-traditional PRO focused on fear of disease recurrence
Time frame: 3 years
Non-traditional PRO focused on disease anxiety and burden
Time frame: 3 years
Non-traditional PRO focused on participatory decision-making style
Vanderbilt University Medical Center
Other
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
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.
Published trials that share one or more normalized conditions with this study.
NCT05309616
Idiopathic Subglottic Stenosis, Idiopathic subglottic tracheal stenosis
New Haven, Connecticut, United States
View Trial DetailsNCT05153668
Idiopathic Subglottic Tracheal Stenosis, Idiopathic subglottic tracheal stenosis
Baltimore, Maryland, United States
View Trial DetailsNCT07228104
Constriction, Pathologic, Idiopathic Subglottic Stenosis
Baltimore, Maryland, United States
View Trial DetailsNCT06161077
Idiopathic Subglottic Tracheal Stenosis, Idiopathic subglottic tracheal stenosis
Baltimore, Maryland, United States
View Trial Details