CETIC-I (CEra Traction Improves Cervical Kyphosis -I)

Status Not yet recruiting

Clinical Trial Summary

The study is a Prospective, Randomized, Single-blinded, Sham device controlled, Parallel Treatment Grouped, Multi-center, Exploratory Clinical Trial to Evaluate Improvement of Cervical Lordosis and Safety of CGM MB-1701 (Spinal warm massage device, Ceragem Master V6) in Subjects with Cervical Kyphosis and Posterior Neck Pain.

Clinical Trial Description

The Cervical Kyphosis are also commonly referred to as "turtle neck syndrome." It refers to the deformation of the neck bone into an inverted C-shape due to abnormalities or degenerative changes, and it is named to mean that the neck is bent like a turtle. This device, Ceragem Master V6 (CGM MB-1701), has been certified as a combination of a personal warmer that can be used to relieve muscle pain by applying constant heat to the human body and a medical vibrator of a device that applies physical energy (vibration, shock, pressure, etc.). Also, the device got approval for use with intermittent pneumatic compression and electrically-powered orthopedics traction. The primary purpose of this clinical trial is to confirm the temporary cervical lordosis angle improvement (height) in subjects with cervical kyphosis through the combined function of the test device. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05469295
Study type	Interventional
Source	Ceragem Inc.
Contact	Hyungsun Kim
Phone	82-10-4597-6672
Email	hyungsun.kim@ceragem.com
Status	Not yet recruiting
Phase	N/A
Start date	May 1, 2023
Completion date	November 30, 2023

View Details

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