DaVinci Registry(Distinctly Assess Vision in Coronary Intervention)

Distinctly Access Vision In Coronary Interventions

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00243438

Enrollment

1300

Registered

2005-10-24

Start date

2003-07-31

Completion date

2005-03-31

Last updated

2009-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Disease

Brief summary

Prospective Internet-Registry, Postmarketing-Surveillance, Registration and Follow-up of patients after Multi-Link VISION™ - Stent Implantation

Detailed description

A Non-Randomized prospective evaluation of the Multi-Link Rx Vision TM Coronary Stent System in the treatment of patients with De novo native coronary artery lesions

Interventions

DEVICEMultilink Vision™ Stent (CE-labeled)

Patients who have diabetes and/or complex lesions and who have had a Multilink Vision™ Stent placed.

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Women and Men Age \>18 years, Intention to treat all stenosis with Multi-Link VisionTM Stents, documented patient consent

Exclusion criteria

* No Multi-Link Vision™ Stent implanted, life expectation \>9 M, cardiogenic shock, STEMI, NSTEMI or unstable angina pectoris with pathologic markers within the last 48 hours, intolerance of Clopidogrel/ Tiklopidin

Design outcomes

Primary

Measure	Time frame
TVF	9 months

Secondary

Measure	Time frame
Mode of death	—
Time to first MI	—
TVR	—
CABG	—

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026