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NCT00846794 Clinical Trial

AcuGraph and Digestive Symptoms

Irritable Bowel Syndrome Clinical Trial

Official title:
Can AcuGraph Differentiate Between Participants With and Without Digestive Symptoms

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00846794
Other study ID # SR1219080169
Secondary ID 400
Status Completed
Phase N/A
First received February 12, 2009
Last updated September 14, 2016
Start date February 2009
Est. completion date March 2010

Study information
Verified date September 2016
Source Logan College of Chiropractic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This research is designed to study the reliability of the results of an AcuGraph in college students and faculty members with reported digestive symptoms

Description:

The specific aim of the study is to test the reliability of the AcuGraph in subjects with irritable bowel syndrome (IBS). The hypothesis is that the AcuGraph will be a reliable method to identify disorders in subjects.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date March 2010
Est. primary completion date March 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Subjects will be required to answer a questionnaire evaluating for a percentage of digestive disorders "disability" based on the subject's answers. If a participant's answers do not qualify as a disability, they will be assigned to the asymptomatic group and will still be examined with an AcuGraph to provide normative data.

Exclusion Criteria:

- heart condition

- kidney disorder

- thyroid disorders

- diabetes

- chronic disease or illness

- neurological diseases

- skin or bleeding disorders

- pregnant

- currently taking drugs or nutritional supplements

- pacemaker and/or

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
United States Logan University, College of Chiropractic Chesterfield Missouri

Sponsors (1)
Lead Sponsor Collaborator
Logan College of Chiropractic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary AcuGraph: computerized device to analyze & document the energetic status of the acupuncture meridians At examination No
Secondary IBS Questionnaire At examination No
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