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Cryospray Therapy for Benign Airway Stenosis (CRYOSTASIS)

Virginia Commonwealth University (VCU) logo

Virginia Commonwealth University (VCU)

Status and phase

Enrolling
Phase 1

Conditions

Stenosis Trachea

Treatments

Device: The truFreeze Spray Cryotherapy
Device: Radial Incision
Device: Ballon dilation

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT06085209
HM20027230

Details and patient eligibility

About

This is a clinical evaluation to assess the effectiveness of cryospray therapy used in addition to current standard of care endoscopic therapies in preventing short term recurrent airway stenosis with a multicentric outcome evaluation. The investigators hypothesize that the addition of SCT to standard endoscopic treatment of benign airway stenosis will result in decreased stenosis recurrence at 6 months as estimated by quantitative radiologic assessment of the stenotic volume.

Full description

Spray cryo treatment of tracheal stenosis has the potential for long-lasting endoscopic management of BCAS and is used as part of routine clinical care by many physicians, but there is a relative paucity of peer-reviewed data, and no randomized controlled trial has been performed. Thus, the study could potentially show that the use of spray cryo therapy could allow patients to undergo fewer procedures to treat this condition, or lengthen the amount of time required in between these procedures, or play a role in the resolution of this condition.

Enrollment

12 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Referral to interventional pulmonology or otorhinolaryngology or thoracic surgery for endoscopic management of suspected benign tracheal stenosis.
  • Significant tracheal stenosis defined by stenosis ≥ 50% of tracheal lumen assessed on chest CT or previous bronchoscopy
  • Able to provide informed consent.
  • Age > 18

Exclusion criteria

  • 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:

    1. Hypoxemia with need for supplemental oxygen ≥ 2L/min by nasal canula
    2. Pneumothorax in the previous 12 months
    3. Severe COPD (defined as a FEV1/FVC < 70% and FEV1 <30% predicted) and/or severe persistent asthma.
    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.
    5. Compromised tissue where significant ulceration or mucosal break is evident in the ablation area or adjacent organs.
    6. Significantly reduced tissue strength caused by prior procedure or pre-existing condition (e.g. PEG tube)
    7. Significantly reduced elasticity of the ablation area (e.g. Marfan's Syndrome)
  • Prior complications with SCT (Spray cryotherapy)

  • Contraindication to rigid bronchoscopy

  • Significant tracheomalacia or alterations in cartilage integrity on CT (Computed Tomography) that would require stent placement or surgical referral.

  • Greater than 1 BCAS intervention, excluding cricotracheal (tracheal surgery) resection, within 6 months before enrollment.

  • Anatomical flow resistance (gas evacuation) where any procedure or anatomy proximal to the ablation site has significantly reduced or restricted the flow area of the lumen creating restriction where gas created from liquid nitrogen cannot adequately vent.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

12 participants in 2 patient groups

Intervention
Experimental group
Description:
Bronchoscopic balloon dilation with radial cuts \& truFreeze spray cryotherapy
Treatment:
Device: Ballon dilation
Device: Radial Incision
Device: The truFreeze Spray Cryotherapy
Standard of care
Active Comparator group
Description:
Bronchoscopic balloon dilation with radial cuts
Treatment:
Device: Ballon dilation
Device: Radial Incision

Trial contacts and locations

1

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Central trial contact

Ramsha Hamid

Data sourced from clinicaltrials.gov

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