A PROSPECTIVE, MULTI-CENTER, SINGLE ARM STUDY TO OBTAIN "REAL WORLD" CLINICAL DATA AND CHARACTERIZE THE ACUTE AND LONG-TERM PERFORMANCE OF THE MICRUSFRAME AND GALAXY COILS FOR THE ENDOVASCULAR TREATMENT OF INTRACRANIAL ANEURYSMS

This Study is
No Longer Enrolling

Description

A Prospective, Multi-Center, Single Arm Study to obtain “Real World” Clinical Data and Characterize the Acute and Long-Term Performance of the Micrusframe and Galaxy Coils for the Endovascular Treatment of Intracranial Aneurysms

Details
Age

Adult

Eligibility

Patient is between 21 and 80 years of age (inclusive) at the time of consent Has an intracranial, saccular aneurysm &#8805;4mm and &#8804;24mm in maximal diameter, ruptured or unruptured, suitable for embolization with coils Hunt and Hess <3 for subjects with ruptured aneurysm Cannot have more than one aneurysm requiring treatment during the course of the study

Phase

Not Applicable - Describes studies without FDA-defined phases, including studies of devices or behavioral interventions.

Type of Study

Observational

Locations

Memorial Hospital Central

Study ID

Protocol Number: 19-6503

More information available at ClinicalTrials.gov: NCT03642639

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