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NCT05703646: e-Yukon

Safety and Clinical Performance of the Yukon Choice PC, Yukon Chrome PC & Yukon Choice Flex Stents in Routine Practice

Status unknown Last updated 27 November 2023
What this trial tests

trial in Ischemic Heart Disease in 5,000 participants. Status unknown.

Timeline
30 March 2023
Primary endpoint
30 March 2026
30 March 2026

Quick facts

Lead sponsorTranslumina GmbH
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment5,000
Start date30 March 2023
Primary completion30 March 2026
Estimated completion30 March 2026
Sites1 location across United Arab Emirates

Conditions studied

Sponsor

Translumina GmbH

Who can join

Adults 18 to 80, any sex, with Ischemic Heart Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this observational study is to collect safety and performance information in the setting of a large-scale clinical registry. Patients meeting the selection criteria will be included, in chronological order of their implantation. This registry does not require any additional procedures, follow-up interventions, or ionizing radiation for patients. The inclusion period is planned to last 2 years, starting in Q1 2023. The study will be complete when data on all patient's follow-up for one year have been collected.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Ischemic Heart Disease

Currently open trials in the same condition.

Other Translumina GmbH 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/NCT05703646.

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