Clinical Trial: A Registry to Gather Real World Use Data on the Cerene® Cryotherapy Device
Study Status: Completed
Recruit Status: RECRUITING
Condition: Heavy Menstrual Bleeding
Study Type: OBSERVATIONAL
Official Title: A Prospective, Observational, Multi-center Study to Gather Real World Use Data on the Effectiveness, Safety, and Site-of-service of the Cerene Device
Brief Summary:
Channel Medsystems, Inc., the manufacturer of the Cerene® Cryotherapy Device (Cerene), is initiating a prospective, observational registry, the Progress registry, to gather data during real world utilization of the Cerene® Cryotherapy Device (Cerene).The primary objective of this registry is to bridge the gap between clinical results and outcomes achieved and reported during the pivotal study of Cerene and those obtained during its real-world use.
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