Viewing Study NCT04154605


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Study NCT ID: NCT04154605
Status: COMPLETED
Last Update Posted: 2025-03-26
First Post: 2019-10-31
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: ClariFix Rhinitis RCT
Sponsor: Stryker Instruments
Organization:

Study Overview

Official Title: ClariFix Rhinitis Randomized Controlled Trial
Status: COMPLETED
Status Verified Date: 2025-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CR RCT
Brief Summary: A randomized, sham-controlled, single-blind study of cryotherapy as a treatment for chronic rhinitis.
Detailed Description: A prospective, multicenter, randomized, sham-controlled, single-blind (participants) study to demonstrate the superiority of treatment with the ClariFix cryotherapy device for reducing symptoms when compared with a sham treatment in patients with chronic rhinitis. The ClariFix device is a Class II FDA-cleared medical device that is intended to be used as a cryosurgical tool for the destruction of unwanted tissue during surgical procedures, including in adults with chronic rhinitis.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: True
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: