Sivasakthi Medical Systems India Private Limited

ANCHOR Trial

ANCHOR Trial

DESCRIPTION

Device

Angiolite

Number of patients

103

Follow up

24 month

Type of lesions

De-novo lesions

OUTCOMES

Primary endpoints

Strut coverage at 3 months

Secondary endpoints
0.07%

In-stent Late Lumen Loss

0%

24 month

Type of lesions

De-novo lesions

CONCLUSIONS

“These low rates are demonstrating an excellent stent performance”

In ANCHOR, Angiolite demonstrated a favorable early healing profile assessed with OCT at 3 and 6-month post PCI.

This was characterized by high rates of strut coverage and very low rates of in-stent LLL.

Imaging data were also coupled with favorable 24-month clinical data characterized by the absence of binary in-stent restenosis, stent thrombosis, myocardial infarction or cardiac death, suggesting a highly efficacy of Angiolite.

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