Treatment of Central Airway Stenoses Using Computer-Assisted Customized 3d Stents TATUM (Three-dimensional Airway Tailored Stent Using Computer-aided Modeling)
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Airway Disease
- Sponsor
- University Hospital, Toulouse
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Percentage of procedures with clinical improvement of the dyspnea
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
Airway stenting is usually efficient to treat central airway obstruction but can lead to severe and potentially lethal complications (stent migration, obstructive granuloma, perforation, and hemoptysis).
3D customized airway stents (computer-aided conception using CT-scan data), perfectly suited to airway anatomy, should improve the tolerance and safety of airway stenting.
We demonstrated in a previous pilot study, dedicated to patients with anatomically complex stenoses the safety of 3D patient-specific stents. These appealing results in highly complex situations suggest the need to evaluate these devices in more common situations.
In this study we aim to test our new generation stents in all patients planned for airway stenting. After computer-assisted segmentation of airways (VGStudioMAX 3.0 software), the stenosis is virtually corrected, leading to the conception of a virtual stent (AnatomikModeling, Toulouse), allowing for the fabrication of a mold using a 3D printer. The stent is then built and sterilized (NOVATECH, Berlin) and inserted during rigid bronchoscopy.
Close follow up is then conducted, including clinical evaluation after one week, three, six and 12 months; spirometry at one week, 3 months, 6 months and 12 months and chest CT-scan at one week.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age \>18 years
- •Informed consent
- •Complex, proximal and symptomatic (dyspnea, cough, peak flow \< 50%, FEV1 \< 50% or post-stenotic infection) airway stenosis
Exclusion Criteria
- •Acute respiratory distress, mechanical ventilation
- •Contraindication to rigid bronchoscopy (severe and irreversible coagulation disorders)
- •Pregnancy
Outcomes
Primary Outcomes
Percentage of procedures with clinical improvement of the dyspnea
Time Frame: 12 months
Percentage of procedures with clinical improvement of the dyspnea with questionnaires of Borg, modified Medical Research Council (mMRC), and Dyspnea 12
Percentage of procedures with clinical improvement of quality of life
Time Frame: 12 months
Percentage of procedures with clinical improvement of quality of life with the VQ11 questionnaire
Secondary Outcomes
- Percentage of procedures with clinical and functional improvement(12 months)
- Percentage of procedures without complications(12 months)
- Percentage of procedures with functional improvement(1 seconde)
- Percentage of procedures with congruence of the stent(1 week)