Actively Recruiting

Phase Not Applicable
Age: 19Years - 65Years
All Genders
Healthy Volunteers
ID07446088

A Single-center, Open-label, Exploratory Clinical Trial to Evaluate the Safety and Efficacy of a Statics Electricity Generator for Electric Stimulation Home Use (CGM MEPC-2401) for Improving Blood Circulation

Led by Ceragem Clinical Inc. · Updated on 2026-03-03

40

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the safety and effectiveness of a static electricity generator device called the Ceragem Celtron Circulation Chair (CGM MEPC-2401) for improving blood circulation in healthy adults aged 19 to 65 years. The study is an open-label, exploratory clinical trial conducted at a single center to assess how this personal electro-potential generator affects blood flow and related parameters. Participants will use the investigational device, the Ceragem Celltron Circulation Chair, for a 30-minute session during which the device applies electric stimulation aimed at enhancing blood circulation. The trial focuses on measuring changes immediately after the application of the device, without any placebo comparison or blinding. During the study, researchers will measure blood flow changes in the dorsal metacarpal vein, capillary diameter, oxygen saturation, and various blood biomarkers before and immediately after the 30-minute device application. Participants will undergo hematology testing and other evaluations to monitor safety and efficacy. The trial will include healthy volunteers with specific body mass index limits and will last through the treatment and immediate assessment period.

CONDITIONS

Brief Title

Electric Stimulation Home Use(CGM MEPC_2401) for Improving Blood Circulation

Who Can Participate

Age: 19Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged between 19 and 65 years
  • Body mass index (BMI) of 30.0 kg/m² or less
  • No abnormal findings on hematology tests (CBC)
Not Eligible

You will not qualify if you...

  • Uncontrolled hypertension despite medication (systolic blood pressure 6150 mmHg or diastolic blood pressure 6100 mmHg at rest)
  • Use of assistive medical devices such as pacemakers, artificial joints, stents, or prostheses
  • History of seizure disorders, loss of consciousness, or high risk of electric shock due to such conditions
  • Presence of ventricular arrhythmias or neurological disorders such as diabetic neuropathy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Single 30-minute application

Participants use the Ceragem Celltron Circulation Chair (CGM MEPC-2401) device at home to improve blood circulation.

1 visit to apply the device

Trial Site Locations

Total: 1 location

1

Wonju Severance Christian Hospital

Wŏnju, South Korea

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Research Team

M

Myeongbae Shin, Researcher

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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