ClinConnect ClinConnect Logo
Search / Trial NCT03957382

Evaluation of Safety and Efficacy of the Accero® (Heal) Stent for Intracranial Aneurysm Treatment

Launched by ACANDIS GMBH · May 17, 2019

Trial Information

Current as of July 24, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying the safety and effectiveness of a device called the Accero® (Heal) Stent, which is used to treat intracranial aneurysms—bulges in blood vessels in the brain that can be dangerous. The goal of the study is to confirm that using this stent is safe for patients who need this type of treatment.

Anyone interested in participating must be treated with the Accero® (Heal) Stent following the manufacturer's instructions. However, people with certain conditions, such as a modified Rankin Scale score greater than 2 (which measures disability) or a Hunt and Hess score greater than 3 (which assesses the severity of a type of bleeding in the brain), will not be eligible. If you join this trial, you can expect close monitoring and care throughout the process to ensure your safety. The trial is currently recruiting participants of all ages and genders.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Any patient treated with ACCERO® (heal) Stent according to IFU and has signed the informed consent
  • Exclusion Criteria:
  • - Patient is participating in another clinical trial

About Acandis Gmbh

Acandis GmbH is a leading medical technology company specializing in the development and commercialization of innovative solutions for interventional neuroradiology and vascular surgery. With a commitment to enhancing patient outcomes, Acandis focuses on designing advanced devices that address complex vascular conditions. The company leverages cutting-edge research and development to create products that prioritize safety and efficacy, while also providing comprehensive support to healthcare professionals. Dedicated to clinical excellence, Acandis actively participates in clinical trials to validate the performance of its solutions and to advance the field of minimally invasive therapies.

Locations

Magdeburg, , Germany

Recklinghausen, , Germany

Berlin, , Germany

Düsseldorf, , Germany

Hamburg, , Germany

Meppen, , Germany

Patients applied

0 patients applied

Trial Officials

Maxim Bester, PD. Dr.

Principal Investigator

Universitätsklinikum Hamburg-Eppendorf

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials