The Study of Slip Pulse Feature Extraction Method Based on the Image Processing Technology for Traditional Chinese Medicine

May 14, 2020 updated by: China Medical University Hospital

The diagnoses processes of Traditional Chinese Medicine (TCM) focus on the following four main types of diagnoses methods consisting of inspection, listening and smelling, inquiry, and palpation. The most important one is palpation also called pulse diagnosis which is to measure wrist artery pulse by TCM doctor's fingers to detect patient's health state. The pulse diagnosis has three parts, namely 'Cun', 'Guan' and 'Chi', with the location. Wrist measurements correspond to different parts of the body's organs.

However, the pulse information is analyzed by TCM doctor's pulse diagnoses process, which is picked only a single waveform from a long-term pulse measured process and often discarded the other waveforms contained in the same information, e.g. Slippery Pulse waveform. The research object of this project is to divide the TCM diagnosis patients into two groups, one is the Slippery Pulse group and the other is a Normal Pulse group, in which 30 cases are collected in each group. The purpose of this project will integrate the TCM doctor's experiences and standardize them in order to construct an effective Slippery Pulse diagnosis system. It could refine Slippery Pulse diagnoses processes and reduce their diagnoses loading by using the proposed approach during this project. Therefore, we could carry out the research on feature extraction method of Slippery Pulse based on the image processing technology. We could extract the pulse characteristics of Slippery Pulse automatically from the many measurement signals and improve the automatic judging ability of the current pulse instrument to the Slippery pulse waveform. Provide important pulse information to the TCM doctors as an important reference for clinical diagnoses.

Study Overview

Status

Unknown

Conditions

Study Type

Observational

Enrollment (Anticipated)

60

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

    • North District
      • Taichung, North District, Taiwan, 40447
        • Recruiting
        • China Medical University Hospital

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

20 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

primary care clinic

Description

Inclusion Criteria:

  1. Already sign test consent permit.
  2. More than 20-year-old.

Exclusion Criteria:

  1. Can not accept acupuncture points stimulators.
  2. Allergic to acupuncture needles.

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Slippery Pulse
Time Frame: 30 minutes in duration.
The purpose of this project will integrate the TCM doctor's experiences and standardize them in order to construct an effective Slippery Pulse diagnosis system.
30 minutes in duration.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Actual)

April 6, 2018

Primary Completion (Anticipated)

April 1, 2021

Study Completion (Anticipated)

April 1, 2021

Study Registration Dates

First Submitted

May 14, 2020

First Submitted That Met QC Criteria

May 14, 2020

First Posted (Actual)

May 19, 2020

Study Record Updates

Last Update Posted (Actual)

May 19, 2020

Last Update Submitted That Met QC Criteria

May 14, 2020

Last Verified

May 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • CMUH107-REC2-050

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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