This is a multicenter, prospective study designed to evaluate performance of the SVS in the REACH SVS control patients. The study is expected to enroll up to 20 patients at up to 12 sites with up to 6 patients per site.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
9
The First Affiliated Hospital of Guangzhou Medical College
Guangzhou, Guangdong, China
Forced expiratory volume at 1 second
Time frame: Three months
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