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Post-Market Clinical Follow-Up Study to Confirm Clinical Performance and Safety of the Codman Enterprise® 2 Vascular Reconstruction Device in the Endovascular Treatment of Intracranial Aneurysms (SUNRISE-2)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT02415010
Recruitment Status : Terminated
First Posted : April 14, 2015
Last Update Posted : December 12, 2019
Information provided by (Responsible Party):
Cerenovus, Part of DePuy Synthes Products, Inc.

No Study Results Posted on for this Study
Recruitment Status : Terminated
Actual Primary Completion Date : June 25, 2019
Actual Study Completion Date : June 25, 2019