Pulmonary DiseaseNCT04996173
Cryospray Therapy Versus Standard of Care for Benign Airway Stenosis (CryoStasis)
A study testing Spray cryotherapy, Ballon Dilation and Radial Incision in people with Pulmonary Disease, run by Vanderbilt University Medical Center at 3 sites in United States.
Trial summary
Benign central airway stenosis (BCAS) is an important cause of both pulmonary morbidity and mortality. Notable causes include post-intubation stenosis, collagen vascular diseases, airway trauma, infectious and idiopathic subglottic stenosis (iSGS). Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Pulmonary Disease
- What is being tested?
- Spray cryotherapy, Ballon Dilation and Radial Incision
- Type of treatment
- Injection or infusion, Medical device
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 40 participants
- Where
- 3 sitesUnited States
- Study dates
- 25 Oct 2021to Apr 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Referral to interventional pulmonology or ENT for endoscopic management of suspected benign tracheal stenosis.
- Significant tracheal stenosis defined by stenosis ≥ 50% of tracheal lumen assessed on chest CT or symptomatology warranting evaluation.
- Able to provide informed consent
- Age > 18
Who cannot join
- Inability to provide informed consent.
- Pregnancy
- Known or suspected malignant central airway stenosis
- Patient has already been enrolled in this study.
- Study subject has any disease or condition that interferes with safe completion of the study including:
- Hypoxemia with need for supplemental oxygen ≥ 2L/min by nasal canula
Show all 13Show fewer
- Recent pneumothorax in the previous 12 months
- Severe COPD (defined as a FEV1/FVC < 70% and FEV1 < 30% predicted) and/or severe persistent asthma.
- Hemodynamic instability with systolic blood pressure <90 mmHg or heart rate > 120 beats/min, unless deemed to be stable with these values by the attending physicians.
- Prior complications with SCT
- Contraindication to rigid bronchoscopy
- Significant tracheomalacia or alterations in cartilage integrity that would require stent placement or surgical referral as assessed by CT imaging.
- Greater then 1 BCAS intervention within 6 months before enrollment
Trial locations and contacts
3 sites in 1 country.
United States3 sites
University of Mississippi Medical Center
Jackson, Mississippi, 39216
Vanderbilt University Medical Center
Nashville, Tennessee, 37232
Virginia Commonwealth University
Richmond, Virginia, 23219
About this study
Official title: Cryospray Therapy for Benign Airway Stenosis: a Randomized Pilot Study
Benign central airway stenosis (BCAS) is an important cause of both pulmonary morbidity and mortality. Notable causes include post-intubation stenosis, collagen vascular diseases, airway trauma, infectious and idiopathic subglottic stenosis (iSGS). Surgery is the preferred definite option; however, the first therapeutic attempt is usually endoscopic to temporarily restore airway patency and symptomatic improvement.
Several endoscopic modalities exist for treatment. Most commonly, thermal or laser therapy to make radial incisions into the stenotic lesion, followed by balloon dilation to increase the area of patency. Clinicians may also inject steroids or antineoplastic agents such as mitomycin C. All of these methods have benefits and associated risks. Symptomatic stenosis frequently reoccurs with these methods. For example, the investigators have been doing 3-4 ballon dilations procedures a week at our institution.
Spray cryotherapy (SCT) is a novel FDA-cleared technique that allows for liquid nitrogen to be delivered through the working channel of a bronchoscope. Few retrospective studies exist without more robust clinical trial data to reduce the risk of bias and support its widespread use. The investigators postulate that SCT and standard of care techniques will improve airway patency volume at six months than the standard of care techniques alone. Some of the proposed advantages include improved wound healing which may translate to less scar tissue and thus improvements in airway patency for a longer duration of time.
Read the detailed description
Airway obstruction is classified into two broad categories based on the underlying etiology: malignant and non-malignant processes. Benign central airway obstruction (BCAO), as the name suggests, is narrowing the tracheal lumen from causes unrelated to underlying endoluminal or extrathoracic cancers. One common mechanism is mechanical stress on the tracheal walls with post-intubated tracheal stenosis (PITS), post-tracheostomy tracheal stenosis (PTTS), and stenosis related to airway stents. Inflammatory disorders such as sarcoidosis, granulomatosis with polyangiitis (GPA), relapsing polychondritis (RPC), amyloidosis are frequently observed. Chronic atypical infections such as Tuberculosis have been implicated, especially in the developing world. Rarely an idiopathic form can develop in women's fifth decade of life, known as idiopathic laryngotracheal stenosis (ILTS).
First-line treatment for BCAO is dependent mainly on the complexity of stenosis. Tracheal sleeve resection with end-to-end anastomosis is recommended for patients with complex lesions and often is the only definitive treatment available for most patients. Bronchoscopic management has been recommended for simple lesions or patients that are not robust surgical candidates. However, the advances in both flexible and rigid bronchoscopic techniques have led to the treatment of more complex lesions. A multidisciplinary and multimodal approach is often necessary to achieve long-lasting airway lumen patency. Current bronchoscopic modalities include balloon dilation, argon plasma coagulation (APC), diode laser or monopolar cautery, stent placement, endoluminal steroids, antineoplastic agents, and Montgomery t-tube placement. Patients will likely need repeat procedures, which can be on the order of several weeks to years.
It is postulated that heat-based modalities may lead to thermal fixation of tissue with reparative healing and fibrotic scarring that may translate to the reoccurrence of fibrotic injury. In addition, using these modalities on patients with high intraoperative oxygen concentrations can lead to airway fires. Spray cryotherapy (SCT) utilizes liquid nitrogen in a metered fashion to flash freeze tissue with subsequent tissue necrosis that has many advantages that heat-based modalities can not offer. The truFreeze System (CSA Medical, Inc., Baltimore, MD, USA) utilizes liquid nitrogen through a 7-french catheter through the working channel of an endoscope. SCT works by rapidly releasing liquid state nitrogen stored at temperatures less than -196C in a circumferential dose area, leading to rapid hypothermic cell death on tissue. As a result, stenotic tissue undergoes intracellular ice crystal formation with eventual rupture and cell death. Unlike slow delivery of liquid nitrogen or contact probe freezing, this rapid expansion allows the extracellular matrix to be largely intact, thus facilitating wound healing without exuberant airway scar. Other potential benefits include using SCT with high oxygen concentrations, improved bleeding, use on materials that may be combustible such as airway stents, and studies showing improved balloon dilation with less chance of airway laceration.
The investigators hypothesize that the addition of SCT to standard endoscopic treatment modalities of BCAO will decrease stenosis recurrence at six months. The investigators plan to measure our primary outcome measure utilizing a novel noninvasive 3D volumetric tracheal reconstruction by CT scan. Secondary outcomes will include changes in symptoms based on a validated questionnaire, physiologic parameters of breathing, and changes in tracheal cell profile with SCT using single-cell RNA sequencing.
Randomization will occur in a 1:1 fashion, with the patients and outcome adjudicators blinded to the underlying intervention. Patients will have a thin cut CT scan within six weeks of the incident procedure, with pulmonary function testing and questionnaire administration within two weeks. The procedure will be done either with an interventional pulmonologist or otolaryngology, depending on the initial referral. General anesthesia is provided with either an endotracheal tube, laryngeal mask airway, rigid bronchoscope, or dedo laryngoscope, depending on the operator's preference and lesion location. The standard of care group will undergo radial cut incisions into the circumferential lesion followed by balloon dilation. The intervention group will undergo two cycles up to 10 second spray time of SCT, followed by radial cuts and balloon dilation. A final spray will be performed after with a standard freeze-thaw cycle. Five patients with idiopathic subglottic stenosis will undergo cryobiopsy. These samples will be compared with controls for changes in cellular profile.
Patients will undergo a thin cut CT scan within 6 weeks after the procedure with repeat physiological parameters and a questionnaire. This CT will act as the personal best to compare to the final CT scan. Finally, at six months, the investigators will repeat these measures with a final CT scan. Throughout the follow-up period, patients will be given access to a mobile application program that will help patients self-monitor peak expiratory flows. If patients undergo a repeat procedure before the 6-month CT, they will be analyzed in an early reintervention subgroup.
- Conditions
- Pulmonary Disease
- Being tested
- Spray cryotherapy, Ballon Dilation, Radial Incision
- Medical subject headings
- Lung Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Spray cryotherapyDevice
A novel FDA cleared technique that allows for Liquid nitrogen (LN2) to be delivered in a metered fashion via a catheter through a flexible bronchoscope.
Ballon DilationDevice
An endoscopic balloon that is inflated with water to pressures between 45 and 131 psi (3 to 9 atm) using a syringe and pressure manometer.
Radial IncisionDevice
Carbon dioxide (CO2) laser or Monopolar electrocautery knife
| Study group | Role | What they receive |
|---|---|---|
| Control | Placebo comparator | Bronchoscopic Balloon Dilation with Radial Cuts Receives: Device: Ballon Dilation; Device: Radial Incision |
| Intervention | Active comparator | Bronchoscopic Balloon Dilation with Radial Cuts \& truFreeze Spray Cryotherapy Receives: Device: Spray cryotherapy; Device: Ballon Dilation; Device: Radial Incision |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percent change in radiographic airway lumen volume at 6 months by CT
The degree of re-stenosis expressed as the percentage of airway lumen volume within the stenotic segment, compared to personal best patency volume on CT scan post procedure.
Measured: 2 weeks post-procedure to 6 months post-procedure.
Secondary outcomes (2)
Change in peak expiratory flow (PEF)
Change in peak expiratory flow (liters per minute) using a mobile device spirometer and in-office pulmonary function testing.
Measured: Measurement intervals: 2 weeks pre-procedure, weekly post procedure until 6 months following
Change in quality of life using the Clinical Chronic Obstructive Pulmonary Disease Questionnaire (COPD CCQ)
The CCQ has been used as a validated quality of life measure in subglottic stenosis. The investigators will send surveys out to patients at set time intervals. The questions are divided into three areas or domains. Symptoms 1, 2, 5, 6; Functional state 7, 8, 9, 10; Mental state 3 and 4. All items are equally weighted by adding score of ten items and dividing by the number ten. The score varies between 0 (very good health status) to 6 (extremely poor health status). Lower overall scores indicate better disease (0) versus a higher score (100) would be severe disease burden.
Measured: Measurement intervals: 2 weeks pre-procedure, 2 weeks post procedure, 3 months and then 6 months post intervention.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Aug 2021
- Study start25 Oct 2021
- Primary completion31 Dec 2026 (estimated)
- Study completionApr 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pulmonary DiseaseStudies of the same condition, open and under way.
- More trials run by Vanderbilt University Medical CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 40 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Vanderbilt University Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- Virginia Commonwealth University, University of Mississippi Medical Center
- Responsible party
- Principal investigator, Fabien Maldonado, Vanderbilt University Medical Center
- Investigators
- Fabien Maldonado, MD, Principal investigator, Vanderbilt University Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04996173
- Sponsor's protocol ID
- 211177
- Status last verified
- Mar 2026
- First submitted
- 19 Jul 2021
- Last updated
- 1 Apr 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 1 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Cryospray Therapy for Benign Airway Stenosis: a Randomized Pilot Study
- ClinicalTrials.gov ID
- NCT04996173
- Acronym / sponsor ID
- 211177
- Conditions
- Pulmonary Disease
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- Vanderbilt University Medical CenterUniversity, hospital or other
- Collaborators
- Virginia Commonwealth University, University of Mississippi Medical Center
- Study start
- 25 Oct 2021 (actual)
- Primary completion
- 31 Dec 2026 (estimated)
- Study completion
- Apr 2027 (estimated)
- First posted
- 9 Aug 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Benign central airway stenosis (BCAS) is an important cause of both pulmonary morbidity and mortality. Notable causes include post-intubation stenosis, collagen vascular diseases, airway trauma, infectious and idiopathic subglottic stenosis (iSGS). Surgery is the preferred definite option; however, the first therapeutic attempt is usually endoscopic to temporarily restore airway patency and symptomatic improvement.
Several endoscopic modalities exist for treatment. Most commonly, thermal or laser therapy to make radial incisions into the stenotic lesion, followed by balloon dilation to increase the area of patency. Clinicians may also inject steroids or antineoplastic agents such as mitomycin C. All of these methods have benefits and associated risks. Symptomatic stenosis frequently reoccurs with these methods. For example, the investigators have been doing 3-4 ballon dilations procedures a week at our institution.
Spray cryotherapy (SCT) is a novel FDA-cleared technique that allows for liquid nitrogen to be delivered through the working channel of a bronchoscope. Few retrospective studies exist without more robust clinical trial data to reduce the risk of bias and support its widespread use. The investigators postulate that SCT and standard of care techniques will improve airway patency volume at six months than the standard of care techniques alone. Some of the proposed advantages include improved wound healing which may translate to less scar tissue and thus improvements in airway patency for a longer duration of time.
Detailed description
Airway obstruction is classified into two broad categories based on the underlying etiology: malignant and non-malignant processes. Benign central airway obstruction (BCAO), as the name suggests, is narrowing the tracheal lumen from causes unrelated to underlying endoluminal or extrathoracic cancers. One common mechanism is mechanical stress on the tracheal walls with post-intubated tracheal stenosis (PITS), post-tracheostomy tracheal stenosis (PTTS), and stenosis related to airway stents. Inflammatory disorders such as sarcoidosis, granulomatosis with polyangiitis (GPA), relapsing polychondritis (RPC), amyloidosis are frequently observed. Chronic atypical infections such as Tuberculosis have been implicated, especially in the developing world. Rarely an idiopathic form can develop in women's fifth decade of life, known as idiopathic laryngotracheal stenosis (ILTS).
First-line treatment for BCAO is dependent mainly on the complexity of stenosis. Tracheal sleeve resection with end-to-end anastomosis is recommended for patients with complex lesions and often is the only definitive treatment available for most patients. Bronchoscopic management has been recommended for simple lesions or patients that are not robust surgical candidates. However, the advances in both flexible and rigid bronchoscopic techniques have led to the treatment of more complex lesions. A multidisciplinary and multimodal approach is often necessary to achieve long-lasting airway lumen patency. Current bronchoscopic modalities include balloon dilation, argon plasma coagulation (APC), diode laser or monopolar cautery, stent placement, endoluminal steroids, antineoplastic agents, and Montgomery t-tube placement. Patients will likely need repeat procedures, which can be on the order of several weeks to years.
It is postulated that heat-based modalities may lead to thermal fixation of tissue with reparative healing and fibrotic scarring that may translate to the reoccurrence of fibrotic injury. In addition, using these modalities on patients with high intraoperative oxygen concentrations can lead to airway fires. Spray cryotherapy (SCT) utilizes liquid nitrogen in a metered fashion to flash freeze tissue with subsequent tissue necrosis that has many advantages that heat-based modalities can not offer. The truFreeze System (CSA Medical, Inc., Baltimore, MD, USA) utilizes liquid nitrogen through a 7-french catheter through the working channel of an endoscope. SCT works by rapidly releasing liquid state nitrogen stored at temperatures less than -196C in a circumferential dose area, leading to rapid hypothermic cell death on tissue. As a result, stenotic tissue undergoes intracellular ice crystal formation with eventual rupture and cell death. Unlike slow delivery of liquid nitrogen or contact probe freezing, this rapid expansion allows the extracellular matrix to be largely intact, thus facilitating wound healing without exuberant airway scar. Other potential benefits include using SCT with high oxygen concentrations, improved bleeding, use on materials that may be combustible such as airway stents, and studies showing improved balloon dilation with less chance of airway laceration.
The investigators hypothesize that the addition of SCT to standard endoscopic treatment modalities of BCAO will decrease stenosis recurrence at six months. The investigators plan to measure our primary outcome measure utilizing a novel noninvasive 3D volumetric tracheal reconstruction by CT scan. Secondary outcomes will include changes in symptoms based on a validated questionnaire, physiologic parameters of breathing, and changes in tracheal cell profile with SCT using single-cell RNA sequencing.
Randomization will occur in a 1:1 fashion, with the patients and outcome adjudicators blinded to the underlying intervention. Patients will have a thin cut CT scan within six weeks of the incident procedure, with pulmonary function testing and questionnaire administration within two weeks. The procedure will be done either with an interventional pulmonologist or otolaryngology, depending on the initial referral. General anesthesia is provided with either an endotracheal tube, laryngeal mask airway, rigid bronchoscope, or dedo laryngoscope, depending on the operator's preference and lesion location. The standard of care group will undergo radial cut incisions into the circumferential lesion followed by balloon dilation. The intervention group will undergo two cycles up to 10 second spray time of SCT, followed by radial cuts and balloon dilation. A final spray will be performed after with a standard freeze-thaw cycle. Five patients with idiopathic subglottic stenosis will undergo cryobiopsy. These samples will be compared with controls for changes in cellular profile.
Patients will undergo a thin cut CT scan within 6 weeks after the procedure with repeat physiological parameters and a questionnaire. This CT will act as the personal best to compare to the final CT scan. Finally, at six months, the investigators will repeat these measures with a final CT scan. Throughout the follow-up period, patients will be given access to a mobile application program that will help patients self-monitor peak expiratory flows. If patients undergo a repeat procedure before the 6-month CT, they will be analyzed in an early reintervention subgroup.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control | Placebo comparator | Device: Ballon Dilation, Device: Radial IncisionBronchoscopic Balloon Dilation with Radial Cuts |
| Intervention | Active comparator | Device: Spray cryotherapy, Device: Ballon Dilation, Device: Radial IncisionBronchoscopic Balloon Dilation with Radial Cuts \& truFreeze Spray Cryotherapy |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Referral to interventional pulmonology or ENT for endoscopic management of suspected benign tracheal stenosis.
- Significant tracheal stenosis defined by stenosis ≥ 50% of tracheal lumen assessed on chest CT or symptomatology warranting evaluation.
- Able to provide informed consent
- Age > 18
Key exclusion criteria (13 listed)
- Inability to provide informed consent.
- Pregnancy
- Known or suspected malignant central airway stenosis
- Patient has already been enrolled in this study.
- Study subject has any disease or condition that interferes with safe completion of the study including:
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Spray cryotherapyA novel FDA cleared technique that allows for Liquid nitrogen (LN2) to be delivered in a metered fashion via a catheter through a flexible bronchoscope. | Device | Intervention |
| Ballon DilationAn endoscopic balloon that is inflated with water to pressures between 45 and 131 psi (3 to 9 atm) using a syringe and pressure manometer. | Device | Control, Intervention |
| Radial IncisionCarbon dioxide (CO2) laser or Monopolar electrocautery knife | Device | Control, Intervention |
Primary outcome
Percent change in radiographic airway lumen volume at 6 months by CT
Time frame: 2 weeks post-procedure to 6 months post-procedure.
The degree of re-stenosis expressed as the percentage of airway lumen volume within the stenotic segment, compared to personal best patency volume on CT scan post procedure.
2 secondary outcomes
Change in peak expiratory flow (PEF)
Time frame: Measurement intervals: 2 weeks pre-procedure, weekly post procedure until 6 months following
Change in quality of life using the Clinical Chronic Obstructive Pulmonary Disease Questionnaire (COPD CCQ)
Time frame: Measurement intervals: 2 weeks pre-procedure, 2 weeks post procedure, 3 months and then 6 months post intervention.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Apr 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Fabien Maldonado, MD principal investigator
Vanderbilt University Medical Center
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Spray cryotherapy, Ballon Dilation and Radial Incision in people with Pulmonary Disease, run by Vanderbilt University Medical Center at 3 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 1 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percent change in radiographic airway lumen volume at 6 months by CT (time frame: 2 weeks post-procedure to 6 months post-procedure.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Apr 2026.