A Registry to Gather Real World Use Data on the Cerene® Cryotherapy Device

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age25+
SponsorChannel Medsystems

About this trial

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.

Eligibility criteria

Qualifiers

Scheduled for a Cerene treatment

25 years of age and older

Provided informed consent to participate in the registry

English speaking

Disqualifiers

Physician discretion

Vulnerable populations

Trial design

Treatments tested in this trial

  • Cerene

Treatment groups

300 Participants
are divided into 1 treatment group

Sponsors and collaborators