Ultra Registry

Treat small aneurysms confidently

The ULTRA Registry is an investigator-initiated prospective, multicenter US registry of patients with small (≤5mm) intracranial aneurysms treated exclusively with Target Ultra and Nano Detachable Coils led by Dr. Gaurav Jindal at the University of Maryland.

Ultra Registry

The evidence is undeniable

At Stryker, our excellence is backed by evidence. When working in small intracranial aneurysms, the ULTRA Registry – an investigator initiated study involving 100 patients – showed that Target Ultra Detachable Coils and Target Nano Detachable Coils had zero coil related complications. For ruptured or unruptured aneurysms, Target Detachable Coils are safe and effective—and the evidence proves it.

Primary endpoints:
Target aneurysm occlusion and recurrence rates

Secondary endpoints:
Device and/or procedure related adverse events, aneurysm
hemorrhage intraoperatively or during follow-up

Mean aneurysm size 3.5 x 3.0 x 2.8mm
Wide neck aneurysms
(Dome-to-neck <2.0)
61%
Average # of coils 2.9 coils
Average packing density 34.3%

100
patients

infographic with people

Mean age of 56 years | 75% female

◼ 48 ruptured      ◼ 52 unruptured

0 coil related complications  0 intraoperative aneurysm ruptures  0 known post-operative aneurysm ruptures  0 crossover to clipping

Raymond l & ll

at one year

"Target Ultra and Nano Coils are outstanding in both safety profile and intraoperative reliability. I’m confident treating small aneurysms with these coils."

Dr. Gaurav Jindal

Data presented as an ePoster at SNIS 2021, manuscript pending journal submission. Presentation available at: https://www.youtube.com/watch?v=c4gbq8JMH2U
The Ultra Registry was an Investigator sponsored research study, funded by a research grant from Stryker.

This content is intended solely for the use of healthcare professionals.

A physician must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient. Stryker does not dispense medical advice and recommends that physicians be trained in the use of any particular product before using it in a procedure. The information presented is intended to demonstrate the breadth of Stryker product offerings. A physician must always refer to the package insert, product label and/or instructions for use before using any Stryker product. Products may not be available in all markets because product availability is subject to the regulatory and/or medical practices in individual markets. Please contact your Stryker representative if you have questions about the availability of Stryker products in your area.