RECRUITING

Cryospray Therapy Versus Standard of Care for Benign Airway Stenosis (CryoStasis)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Cryospray Therapy for Benign Airway Stenosis: a Randomized Pilot Study

Quick Facts

Study Start:2021-10-25
Study Completion:2026-04
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04996173

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Referral to interventional pulmonology or ENT for endoscopic management of suspected benign tracheal stenosis.
  2. 2. Significant tracheal stenosis defined by stenosis ≥ 50% of tracheal lumen assessed on chest CT or symptomatology warranting evaluation.
  3. 3. Able to provide informed consent
  4. 4. Age \> 18
  1. 1. Inability to provide informed consent.
  2. 2. Pregnancy
  3. 3. Known or suspected malignant central airway stenosis
  4. 4. Patient has already been enrolled in this study.
  5. 5. Study subject has any disease or condition that interferes with safe completion of the study including:
  6. 1. Hypoxemia with need for supplemental oxygen ≥ 2L/min by nasal canula
  7. 2. Recent pneumothorax in the previous 12 months
  8. 3. Severe COPD (defined as a FEV1/FVC \< 70% and FEV1 \< 30% predicted) and/or severe persistent asthma.
  9. 4. 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.
  10. 5. Prior complications with SCT
  11. 6. Contraindication to rigid bronchoscopy
  12. 7. Significant tracheomalacia or alterations in cartilage integrity that would require stent placement or surgical referral as assessed by CT imaging.
  13. 8. Greater then 1 BCAS intervention within 6 months before enrollment

Contacts and Locations

Study Contact

Ankush Ratwani, MD
CONTACT
615-322-3412
ankush.ratwani@vumc.org
Briana Swanner
CONTACT
615-574-1576
briana.swanner@vumc.org

Principal Investigator

Fabien Maldonado, MD
PRINCIPAL_INVESTIGATOR
Vanderbilt University Medical Center

Study Locations (Sites)

University of Mississippi Medical Center
Jackson, Mississippi, 39216
United States
Vanderbilt University Medical Center
Nashville, Tennessee, 37232
United States
Virginia Commonwealth University
Richmond, Virginia, 23219
United States

Collaborators and Investigators

Sponsor: Vanderbilt University Medical Center

  • Fabien Maldonado, MD, PRINCIPAL_INVESTIGATOR, Vanderbilt University Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-10-25
Study Completion Date2026-04

Study Record Updates

Study Start Date2021-10-25
Study Completion Date2026-04

Terms related to this study

Additional Relevant MeSH Terms

  • Pulmonary Disease