Atrial Septal Defect Clinical Trial
Official title:
A Randomized Multicenter Comparison Trial to Evaluate the Effectiveness and Safety of the Guidewire for Echo-guided Interventions in Treating ASD
Prospective randomized multicenter trial of about 100 subjects enrolled in 3-5 centers. Patients will be randomized to two groups in equal proportion (50 in each). To precise the function of this device on reducing technical difficulties and conquering learning curves, it is required that the doctor should be able to independently do echo-guided percutaneous interventions and his cases should be more than 20 but less than 100. Experimental group is allocated to use novel interventional guidewire for echocardiography guided percutaneous interventions for ASD, control group will be treated by cook lunderquist guidewire. If echo-guided procedure does not work well, the procedure will be immediately replaced by conventional procedure guided by radiology. To evaluate the effectiveness and safety comprehensively, variables are defined as success rate, duration of procedure, times of arrhythmia, times of misguided to tricuspid valve, cardiac perforation, cardiac tamponed, complications in peripheral vessels etc.
1. This is a prospective blinded randomized multicenter comparison clinical trial followed
the design of superiority trial to compare the effectiveness and safety of the guidewire
for echo-guided interventions designed by Hangzhou Dexin Medical Technological Company
with other similar products.
2. This trial will enroll about 100 subjects from 3-5 centers. Patients will be randomized
to two groups in equal proportion (50 in each). Proposal recruiting period is 18 months
and follow-up will be performed for 30 days.
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