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Cera™ Vascular Plug System Post-Market Clinical Follow-Up

NCT06099015 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 132

Last updated 2026-04-23

No results posted yet for this study

Summary

The objective of the study is to collect and evaluate clinical data on patients of the Lifetech Cera™ Vascular Plug System to:

* confirm the performance
* confirm the safety
* identify previously unknown side-effects
* monitor the identified side-effects (related to the procedures or to the medical devices)
* identify and analyse emergent risks

Conditions

  • Aneurysm
  • Endoleak
  • Pulmonary Arteriovenous Malformation
  • Portal Hypertension
  • Arteriovenous Fistula
  • Splenic Laceration

Interventions

DEVICE

Cera™ Vascular Plug System

The Cera™ Vascular Plug System is composed of Cera™ Vascular Plug and its accessory Introducer Kit. The Cera™ Vascular Plug is a self-expandable, cylindrical Ni-Ti wire mesh device.

Sponsors & Collaborators

  • Lifetech Scientific (Shenzhen) Co., Ltd.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-21
Primary Completion
2026-12-31
Completion
2027-12-31

Countries

  • Germany
  • Italy
  • Turkey (Türkiye)

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 NCT06099015 on ClinicalTrials.gov