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RECRUITING
NCT05922657

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

Sponsor: Channel Medsystems

View on ClinicalTrials.gov

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.

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

Key Details

Gender

FEMALE

Age Range

25 Years - Any

Study Type

OBSERVATIONAL

Enrollment

300

Start Date

2023-06-09

Completion Date

2027-12-31

Last Updated

2025-12-16

Healthy Volunteers

No

Interventions

DEVICE

Cerene

Real world use of Cerene.

Locations (2)

Axia Women's Health / Rubino OB/GYN Group

West Orange, New Jersey, United States

Seven Hills Women's Health Centers

Cincinnati, Ohio, United States