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Study identifier: NCT06849635 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Cera™ ASD Occluder Post-Market Clinical Follow-Up Study

Condition: Atrial Septal Defect  ·  Sponsor: Lifetech Scientific (Shenzhen) Co., Ltd.

PhaseN/A
Planned participants139
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

The objective of this post-market study is to: * collect real-word clinical data and confirm the long-time safety and performance of the Lifetech Cera™ ASD Occluder * identify previously unknown side-effects

This description comes directly from the study's public registry record.

Talk to the study team

KaDirr Shemsi  ·  +86-176-2130-9203  ·  kadirr@lifetechmed.com

Jiaxuan Fu  ·  86+13973207184  ·  fujiaxuan@lifetechmed.com

Always discuss trial participation with your own doctor first.

Locations (6)

G.V.M.Carint HospitalMyszków, PolandNot Yet Recruiting
Centre for Invasive Cardiology, Electrotherapy and Angiology G.V.M.Carint-OswiecimOświęcim, PolandNot Yet Recruiting
Subcarpathian Centre for Cardiovascular Intervention G.V.M.Carint -SanokSanok, PolandNot Yet Recruiting
Polish-American Heart Clinics, Heart and Vascular Center in Tychy, American Heart of Poland GroupTychy, PolandRecruiting
Polish-American Heart Clinics 1st Department of Invasive Cardiology and Heart Failure in Ustroń, AHoP GroupUstroń, PolandNot Yet Recruiting
Dr. Tytus Chałubiński County HospitalZakopane, PolandNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06849635