- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01545960
Evaluating Acupuncture Points With Scanning Kelvin Probe
March 2, 2012 updated by: Andrew A. Ahn, Massachusetts General Hospital
Scanning Kelvin Probe Measurements of Acupuncture Point
The purpose of this study is to characterize the surface electrical potential of acupuncture points with a Scanning Kelvin Probe.
Study Overview
Status
Suspended
Intervention / Treatment
Detailed Description
Acupuncture points are anatomical structures described by traditional Chinese medicine.
To this day, however, their scientific and Western anatomical characterizations remain unclear.
Past studies have suggested that acupuncture points are distinct electrically (increased electrical conductivity).
To evaluate this claim, this study uses a Scanning Kelvin Probe to study the electrical potential of three acupuncture points and their respective adjacent controls in 24 healthy individuals.
The Scanning Kelvin Probe is a novel device that measures the electrical potential of skin without actually touching the skin surface.
Study Type
Observational
Enrollment (Anticipated)
24
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Massachusetts
-
Charlestown, Massachusetts, United States, 02129
- Massachusetts General Hospital - Martinos Center for Biomedical Imaging
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Healthy volunteers
Description
Inclusion Criteria:
- Individuals without chronic medical condition requiring daily medications (hypertension, diabetes, hypothyroidism, etc).
Exclusion Criteria:
- Individuals with autonomic disorders (sweating irregularities), skin disorders, extensive burns/scars on the hand, tremors, neuromuscular conditions, restless leg syndrome, movement disorders, and implanted cardiac defibrillator/pacemaker
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy Volunteers
|
No actual interventions will be administered for this study.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Electrical Potential at Acupuncture points
Time Frame: One day
|
Scanning Kelvin Probe measurements of electrical potentials at 3 predetermined acupuncture points.
|
One day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2011
Primary Completion (Anticipated)
August 1, 2012
Study Completion (Anticipated)
August 1, 2012
Study Registration Dates
First Submitted
March 2, 2012
First Submitted That Met QC Criteria
March 2, 2012
First Posted (Estimate)
March 7, 2012
Study Record Updates
Last Update Posted (Estimate)
March 7, 2012
Last Update Submitted That Met QC Criteria
March 2, 2012
Last Verified
March 1, 2012
More Information
Terms related to this study
Other Study ID Numbers
- 5R21AT005249-03 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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