Condition: Pneumothorax · Sponsor: Hangzhou Broncus Medical Co., Ltd.
Study Objective: To evaluate the feasibility and safety of the disposable endobronchial silicon spigots for treating refractory pneumothorax and to preliminarily assess its efficacy, providing domestic experience for the development and clinical application of bronchial occlusion. Study Population: Patients intended to receive selective bronchial occlusion technology for the treatment of refractory pneumothorax. Sample Size: This study is a preliminary exploration of the application value of the disposable endobronchial silicon spigots occlusion technology in refractory pneumothorax. The sample size has not been strictly calculated, and it is expected to include 10 patients. Study Design: This study is an exploratory, single-group, single-center clinical study.
This description comes directly from the study's public registry record.
Liheng Xie · +86-13916444591 · medicalaffairs@broncuschina.com
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| The Second Affiliated Hospital of Fujian Medical University | Quanzhou, Fujian, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06515015