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Trials / Completed

CompletedNCT05893758

Lifetech Cera™ PFO Occluder Post-Market Clinical Follow-Up

A Real-world Registry Assessing the Clinical Use of the Lifetech Cera™ PFO Occluder

Status
Completed
Phase
Study type
Observational
Enrollment
94 (actual)
Sponsor
Lifetech Scientific (Shenzhen) Co., Ltd. · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The objective of this post-market registry is to assess the clinical use of the Lifetech Cera™ PFO Occluder in a real-world and on-label fashion.

Conditions

Interventions

TypeNameDescription
DEVICEThe Cera™ PFO OccluderThe Cera™ PFO Occluder is a percutaneous, transcatheter closure device for the non-surgical closure of Patent Foramen Ovale (PFO).

Timeline

Start date
2023-08-10
Primary completion
2024-02-01
Completion
2024-02-01
First posted
2023-06-08
Last updated
2024-08-30

Locations

5 sites across 1 country: Poland

Source: ClinicalTrials.gov record NCT05893758. Inclusion in this directory is not an endorsement.

Lifetech Cera™ PFO Occluder Post-Market Clinical Follow-Up (NCT05893758) · Clinical Trials Directory