Efficacy of Microcurrent Therapy for Treatment of Knee Pain

NCT ID: NCT03511014

Last Updated: 2018-04-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-03-01

Study Completion Date

2019-02-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Acute Knee Pain

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

microcurrent

Group Type EXPERIMENTAL

Microcurrent

Intervention Type DEVICE

Micrucurrent will be apply

control

Group Type SHAM_COMPARATOR

Microcurrent

Intervention Type DEVICE

Micrucurrent will be apply

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Microcurrent

Micrucurrent will be apply

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

21 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Elon University, Department of Physical Therapy Education

INDUSTRY

Sponsor Role collaborator

Omron Healthcare Co., Ltd.

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Omron healthcare Co.,Ltd.

Mukō, , Japan

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Japan

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Shozo Takamatsu

Role: primary

+81-75-925-2043

Keisuke Yamada

Role: backup

+81-75-925-2043

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

HI794-0001

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.