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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03187782
Other study ID # TH-IRB-0014-0002
Secondary ID
Status Completed
Phase N/A
First received May 25, 2017
Last updated June 13, 2017
Start date February 2014
Est. completion date February 2015

Study information

Verified date June 2017
Source Taipei Hospital, Taiwan
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The mechanism led to the dysmenorrhea can be understood more clearly and one may have a better idea to treat the disease in the future.


Description:

Background: Pulse diagnosis of the dysmenorrhea patients before and after acupuncture treatment on the acupoint San Yin Jiao (SP6) were performed so that the mechanism led to the pain can be understood more clearly and one may have a better idea to treat the disease in the future.

Methods: Fifteen women participated in the study voluntarily. They have first to fill in the form of Visual Analogue Scale (VAS) for pain. Then the pulse of the subjects were measured by ANSWatch before and after acupuncture. All meridians can be assessed by analyzing the pulse spectra through Fast Fourier Transform (FFT) of the original pulse data. The significant change of amplitude in certain harmonics which corresponds to a specific meridian after acupuncture treatment can be selected out.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date February 2015
Est. primary completion date February 2015
Accepts healthy volunteers
Gender Female
Age group 12 Years to 55 Years
Eligibility Inclusion Criteria:

- The inclusion criteria of the subjects were the presence of pain during menstruation or three days before it. It needed to recheck if the menstrual cycle appeared within three days after recruiting if dysmenorrhea attacked before menstruation.

Exclusion Criteria:

- The exclusion criterion was that subjects did not take pain killers in the 12 hours before measurement.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
ANSWatch


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Taipei Hospital, Taiwan

Outcome

Type Measure Description Time frame Safety issue
Primary Patients' radial artery pulses. Change is being assessed. Get subjects' pulses by ANSWatch Measure subjects' radial artery pulses before and after acupuncture in 10 minutes respectively.
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