the objective of the Israeli MGurad Registry is to evaluate the 'Real World' Clinical
Performance of the InspireMD MGuard Coronary Stent System
Device: MGuard Coronary Stent system
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Locations near you
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Full eligibility criteria for NCT00922337
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Patient is > 18 years of age
The patient has consented to participate by signing the "Patient Informed Consent Form"
Patient is suitable for implantation of one or more MGuard Stent System in one or more target lesions
Target lesion(s) are according to the Indications for Use and Israeli regulatory approval of the MGuard Stent System
The patient is willing and able to cooperate with registry procedures and required follow up
Heavily calcified target lesions
Target lesions with side branch bigger then 2.5mm
Target lesions which are distal to newly stented lesion (less than 1 month).
Women with known pregnancy
Current medical condition with a life expectancy of less than 12 months
Patients with medical conditions that preclude the follow-up as defined in the protocol or that otherwise limits study participation
All locations for NCT00922337
Asaf Harofe Medical Center
View full eligibility
Tris trial is registered with FDA with number: NCT00922337. The sponsor of the trial is InspireMD and it is looking for 86 volunteers for the current phase.
Official trial title: A Prospective, Observational, Multicenter Registry To Evaluate the 'Real World' Clinical Performance of the MGuard Coronary Stent System
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