Geneva, April 27 -- International Clinical Trials Registry received information related to the study (NCT07529028) titled 'Safety and Efficacy of the AbsnowTM II Absorbable Atrial Septal Defect Closure System for Atrial Septal Defect Closure Therapy' on April 7.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).
Primary Sponsor: Lifetech Scientific (Shenzhen) Co., Ltd.
Condition:
Atrial Septal Defect
Intervention:
Device: Absnow II Absorbable Atrial Septal Defect Occluder System
Recruitment Status: Not recruiting
Phase: N/A
Date of First Enrollment: April 2026
Target Sample Size: 236
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