truFreeze Spray Cryotherapy
DeviceTruFreeze Spray CryoTherapy using liquid nitrogen
NCT Number: NCT02572557
Rationale: Spray cryotherapy (SCT) using liquid nitrogen has been safely and effectively used in the esophagus, airways and pleura. Treatment with SCT for central airway stenosis may provide an effective, and more durable and perhaps safer alternative to the current therapeutic modalities.
Objectives:
1. To investigate the feasibility of using Spray cryotherapy (SCT) for the treatment of malignant and benign central airway disease. 2. To investigate the safety of using Spray cryotherapy (SCT) for the treatment of malignant and benign central airway disease. 3. To investigate the efficacy of using Spray cryotherapy (SCT) for the treatment of malignant and benign central airway disease.
Study design: This study will be a prospective, single arm, open label intervention study performed at the University Medical Center Groningen, The Netherlands Study population: The study population exists of 25 patients with malignant or benign central airway disease. Patients in which current treatment options are regarded to be suboptimal can be included in the study.
Intervention: TruFreeze Spray CryoTherapy
Main study parameter:
Feasibility is defined as being able to apply the SCT as planned in one, or more bronchoscopies according to the instructions for use (IFU).
Secondary study parameters:
Safety will be assessed by capturing all adverse events (AEs) that occur 1) during the SCT procedure, and 2) all AEs that occur until hospital discharge.
Efficacy will be measured using 1) patient reported outcomes (questionnaires), 2) percentage improvement in airway stenosis, 3) durability of treatment effect, 4) need to re-intervene with other therapies because of treatment failure.
Nature and extent of the burden, risks and benefit associated with participation.
Patients that will be recruited and participate in this prospective clinical trial have a severe central airway disease which is highly symptomatic for which current available therapies are either very difficult to perform, are hazardous, have no real benefit, or just simply not available yet. The current treatment risks of this patient group are high, especially in the patients where the airway patency is at risk. The main additional risk associated with the use of SCT is the occurrence of a pneumothorax. Patients participating will adhere to their current medical care, with the one addition of a voluntary follow-up bronchoscopy after SCT.
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Interventional
Not applicable
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion Criterium:
Exclusion criteria
TruFreeze Spray CryoTherapy using liquid nitrogen
TruFreeze Spray CryoTherapy using liquid nitrogen
Time frame: During bronchoscopy procedure
Feasibility is defined as being able to apply the SCT as planned in one, or more bronchoscopies according to the instructions for use
Time frame: During bronchoscopy procedure
Safety will be assessed by capturing all adverse events (AEs) that occur during the SCT procedure.
Time frame: Up to 5 days after treatment
Safety will be assessed by capturing all adverse events (AEs) that occur until hospital discharge.
Time frame: 4 weeks follow up
Efficacy will be measured using patient reported outcomes (questionnaires).
Time frame: 4 weeks follow up
Efficacy will be measured by percentage improvement in airway stenosis.
Time frame: 4 weeks follow up
Efficacy will be measured by durability of treatment effect (time in weeks)
Time frame: 4 weeks follow up
Efficacy will be measured by the need to re-intervene with other therapies because of treatment failure.
University Medical Center Groningen
Other
A Prospective Evaluation of Spray Cryotherapy in Patients With Malignant and Benign Central Airway Disease
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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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