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

NCT06849635 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 139

Last updated 2025-03-06

No results posted yet for this study

Summary

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

Conditions

  • Atrial Septal Defect

Sponsors & Collaborators

  • Lifetech Scientific (Shenzhen) Co., Ltd.

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-03
Primary Completion
2025-12-31
Completion
2026-02-28

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06849635 on ClinicalTrials.gov