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Evaluating Acupuncture Points With Scanning Kelvin Probe

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ClinicalTrials.gov Identifier: NCT01545960
Recruitment Status : Suspended (Adjusting minor software glitches)
First Posted : March 7, 2012
Last Update Posted : March 7, 2012
Sponsor:
Information provided by (Responsible Party):
Andrew A. Ahn, Massachusetts General Hospital

Brief Summary:
The purpose of this study is to characterize the surface electrical potential of acupuncture points with a Scanning Kelvin Probe.

Condition or disease Intervention/treatment
Healthy Individuals Acupuncture Points Electrical Potential Other: not applicable in this study

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
Estimated Enrollment : 24 participants
Observational Model: Case Control
Time Perspective: Cross-Sectional
Official Title: Scanning Kelvin Probe Measurements of Acupuncture Point
Study Start Date : August 2011
Estimated Primary Completion Date : August 2012
Estimated Study Completion Date : August 2012

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Group/Cohort Intervention/treatment
Healthy Volunteers Other: not applicable in this study
No actual interventions will be administered for this study.



Primary Outcome Measures :
  1. Electrical Potential at Acupuncture points [ Time Frame: One day ]
    Scanning Kelvin Probe measurements of electrical potentials at 3 predetermined acupuncture points.


Biospecimen Retention:   Samples With DNA
Whole Blood


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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Healthy volunteers
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01545960


Locations
United States, Massachusetts
Massachusetts General Hospital - Martinos Center for Biomedical Imaging
Charlestown, Massachusetts, United States, 02129
Sponsors and Collaborators
Massachusetts General Hospital
Investigators
Principal Investigator: Andrew C. Ahn, MD, MPH Massachusetts General Hospital

Responsible Party: Andrew A. Ahn, Assistant Professor, Massachusetts General Hospital
ClinicalTrials.gov Identifier: NCT01545960     History of Changes
Other Study ID Numbers: 5R21AT005249-03 ( U.S. NIH Grant/Contract )
First Posted: March 7, 2012    Key Record Dates
Last Update Posted: March 7, 2012
Last Verified: March 2012