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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03511014
Other study ID # HI794-0001
Secondary ID
Status Recruiting
Phase N/A
First received April 17, 2018
Last updated April 17, 2018
Start date March 1, 2018
Est. completion date February 1, 2019

Study information

Verified date April 2018
Source Omron Healthcare Co., Ltd.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect of microcurrent therapy at the knee pain.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date February 1, 2019
Est. primary completion date July 31, 2018
Accepts healthy volunteers No
Gender All
Age group 21 Years to 70 Years
Eligibility Inclusion Criteria:

- Pain perceived as a minimum of 3/10 on a 0-10 pain scale

- No phobia of electrical stimulation

- No pain or anti-inflammatory medication will be taken during study

- Injury that began prior to 6-weeks ago before the onset of pain

- Grade II soft tissue injury

Exclusion Criteria:

- Pregnancy

- Diabetes Mellitus

- Neuropathy

- Smoker

- Uncontrolled HTN

- Past surgery in the region to be treated by microcurrent

- Arthritis (RA) in the area to be treated by microcurrent

- Cardiovascular disease

- Allergic to tape/electrodes

- Ligament injury

- Patella Femoral Pain Syndrome (Anterior knee pain)

- Dementia

- Grade III soft tissue injury

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Microcurrent
Micrucurrent will be apply

Locations

Country Name City State
Japan Omron healthcare Co.,Ltd. Muko

Sponsors (2)

Lead Sponsor Collaborator
Omron Healthcare Co., Ltd. Elon University, Department of Physical Therapy Education

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numeric Pain scale (NRS) for pain (0-10) 4weeks