About this trial
This study employs a multicenter, randomized controlled trial method, where patients meeting the inclusion criteria for subglottic stenosis are randomly divided into two groups. These groups are respectively undergoing translaryngeal endoscopic mucosal injection and ultrasound-guided injection of triamcinolone treatment. The comparison will focus on various indicators such as therapeutic effect, incidence of adverse reactions, treatment costs, and hospital resource utilization between the two groups. The safety and effectiveness will be compared to determine the relative merits of the two treatment methods.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
1: "Diagnosed with subglottic stenosis through laryngoscopic examination or imaging studies such as CT."
2: "Experiencing symptoms related to subglottic stenosis, such as breathing difficulties, hoarseness, etc."
Disqualifiers
1: "Severe cardiopulmonary dysfunction, patients extremely debilitated and unable to tolerate the procedure."
2: "Patients allergic to lidocaine, midazolam, triamcinolone, or any of their components."
3: "Pregnant or lactating women."
4: "Unstable angina, congestive heart failure, severe bronchial asthma."
Trial design
Parallel
Treatments tested in this trial
Ultrasound-Guided
Procedure/SurgeryUltrasound-Guided Triamcinolone Injection
Translaryngeal Endoscopic Mucosal Injection
Procedure/SurgeryTranslaryngeal Endoscopic Mucosal Injection of Triamcinolone
Treatment groups
Trial outcomes
Primary outcomes
Incidence of Short-Term Postoperative Complications
Follow-up on short-term postoperative complications (including pneumothorax, bleeding, wound infection, pain, fever, etc.)
Secondary outcomes
Overall medical expenses incurred by patients
Overall medical expenses incurred
Sponsors and contacts
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