Comparison of the Safety and Economics of Translaryngeal Endoscopic Mucosal Injection Versus Ultrasound-Guided Injection of Triamcinolone for the Treatment of Subglottic Stenosis: a Multicenter, Randomized Controlled Study.

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
China
China-Japan Friendship Hospital
RECRUITING
Beijing
Contact Information
Primary
Gang Hou, PI
hougangcmu@163.com
01084206250
Backup
Mingming Deng, Phd
isdeng1017@163.com
18801336854
Time Frame
Start Date: 2024-03-10
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 40
Treatments
Experimental: Ultrasound-Guided Triamcinolone Injection Treatment Group
Ultrasound-Guided Triamcinolone Injection for the Treatment of Subglottic Stenosis
Experimental: Translaryngeal Endoscopic Mucosal Injection of Triamcinolone Treatment Group
Translaryngeal Endoscopic Mucosal Injection for the Treatment of Subglottic Stenosis
Related Therapeutic Areas
Sponsors
Leads: China-Japan Friendship Hospital

This content was sourced from clinicaltrials.gov

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