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

NCT05469295 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-02-09

No results posted yet for this study

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.

Conditions

  • Cervical Kyphosis
  • Cervical Lordosis
  • Kyphosis

Interventions

DEVICE

CGM MB-1701 Sham device treatment

It is manufactured in the same way as the test device and the operation pattern. However, the actual effect of the massage is minimized.

DEVICE

CGM MB-1701 device treatment

This is a pre-approved motorized traction device.

Sponsors & Collaborators

  • Ceragem Clinical Inc.

    lead INDUSTRY

Principal Investigators

  • Yong Il Shin, MD · Pusan National University Yangsan Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-09
Primary Completion
2024-07-26
Completion
2024-07-26

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05469295 on ClinicalTrials.gov