Airway Stenosis
Conditions
Brief summary
The primary aim of this research is to assess the efficacy and safety of the bronchial navigation positioning equipment in assisting stent implantation for malignant central airway stenosis while guaranteeing the safety of the participants and the scientificity of the clinical trial.
Interventions
PROCEDUREUnicorn system
Patients with airway stenosis undergo stent placement with the help of RBS.
Sponsors
Guangzhou Medical University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients are eligible only if they fulfill all of the following criteria: 1. Age ≥ 18 years, regardless of gender; 2. Patients voluntarily consent to airway stent implantation and meet the requirements for airway stent implantation under general anesthesia; 3. Confirmed as having malignant central airway stenosis through bronchoscopy and being ineligible for surgery or refusing surgery, and in need of airway stent implantation. Patients should be able to understand the purpose of the trial, demonstrate good compliance with the examinations and follow-ups, and voluntarily participate in the clinical trial and sign the informed consent form.
Exclusion criteria
* Patients fulfilling any of the following criteria will be excluded from this study: 1. Severe dysfunction of the heart, lungs, liver, or kidneys, intolerant of bronchoscopic treatment; 2. Apparent coagulation dysfunctions; 3. Pregnant or lactating women, or participants with a pregnancy plan during the study period; 4. Patients with implanted cardiac pacemakers, implanted defibrillators, or other active implants; 5. Participants allergic to photosensitizers or anesthetics, or with a history of multiple severe allergies or hereditary allergies; 6. Participants who have participated in or are currently participating in drug clinical trials within the past 3 months, or in other medical device clinical trials within the past 30 days; Other circumstances that the investigator considers inappropriate for participation in this clinical trial.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The success rate of stent placement | During the bronchoscopy | The success rate of stent placement = (The number of patients with successful stent placement / The number of patients undergoing stent placement surgery) × 100% Successful placement: The stent is placed in the appropriate position without displacement, and the upper and lower ends of the stent are unobstructed. |
Contacts
Primary ContactChanghao Zhong
Outcome results
None listed