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NCT05174442

ACCESS Registry: A Post Market Follow-up Study to Monitor the Safety, Performance and Usability of Occlutech Accessory Medical Devices

Recruiting now Last updated 4 December 2025
What this trial tests

trial in Heart Diseases in 685 participants. Currently enrolling.

Timeline
14 October 2021
Primary endpoint
1 January 2027
1 January 2027

Quick facts

Lead sponsorOcclutech International AB
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment685
Start date14 October 2021
Primary completion1 January 2027
Estimated completion1 January 2027
Sites36 locations across Turkey (Türkiye), Germany

Conditions studied

Sponsor

Occlutech International AB — full company profile →

Who can join

Eligibility, any sex, with Heart Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The registry is an international, multicenter, non-randomized, non-invasive study to assess the safety, performance and usability of the Occlutech Accessories "Occlutech Delivery Set (ODS), Occlutech Pistol Pusher (OPP), Occlutech Occlusions-Pusher (OOP) and Occlutech Sizing Balloon (OSB)" used for implantation procedures (catheter-based interventions) of cardiac implants via completing surveys (questionnaires) for the accessory medical devices by the investigators.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Heart Diseases

Currently open trials in the same condition.

Other Occlutech International AB trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05174442.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing