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Immediate Effects of Proximal and Distal Acupoints on the RPPW in Patients With KOA: a Randomized Controlled Trial

Primary Purpose

Knee Osteoarthritis

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Acupuncture
Sponsored by
China Medical University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis focused on measuring knee osteoarthritis, acupuncture, radial pressure pulse-wave, spectral energy

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients meet at least three out of the following six conditions:

  • Any gender aged 50 years or above;
  • Have less than 30 mins of morning stiffness;
  • Crepitus on active motion;
  • Bony tenderness;
  • Bony enlargement;
  • No palpable warmth.

Exclusion Criteria:

  • Subjects who are unable to walk.
  • Malignancy,
  • Any acute medical condition,
  • Poorly controlled diabetes or hypertension,
  • A motor or sensory nerve defect,
  • Blood clotting disease,
  • Mental illness,
  • Dementia,
  • Mental retardation or other abnormal person on the organic mind.
  • Subjects with intra-articular solid or hyaluronic acid injection in the past 3 months.
  • Knee surgery,
  • Knee trauma,
  • Congenital knee deformation,
  • Severe knee varus or valgus deformation,
  • Endocrine,metabolic, infectious, inflammatory, secondary degenerative knee arthritis caused by problems with rheumatic immune diseases.
  • Subjects who are hypersensitive to needles.
  • Subjects who are unwilling to cooperate or sign the subject consent.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Placebo Comparator

    Arm Label

    proximal acupoints

    distal acupoints

    sham acupoints

    Arm Description

    Acupuncture needles will be administered at proximal acupoints

    Acupuncture needles will be administered at distal acupoints

    Sham acupuncture needles will be administered in the abdominal sham acupoints.

    Outcomes

    Primary Outcome Measures

    Assessment of Radial Pressure Pulse-wave at cunkou (1)
    Assessment of Radial Pressure Pulse-wave at cunkou ie at Cun, Guan & Chi of both hands before and after the intervention using Pulse Sphygmograph at 10 min before acupuncture.
    Assessment of Radial Pressure Pulse-wave at cunkou (2)
    Assessment of Radial Pressure Pulse-wave at cunkou ie at Cun, Guan & Chi of both hands before and after the intervention using Pulse Sphygmograph at 10 min after acupuncture.

    Secondary Outcome Measures

    Range of knee motion
    Range of knee motion will be examined by a goniometer.
    Visual analog scale (VAS)
    The intensity of pain is measure using VAS for pain. It is incorporated into the questionnaire with a scale of 0 (no pain) to 10 (worst pain possible)
    The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
    A questionnaire developed to evaluate the condition of patients with osteoarthritis of the knee and hip, including pain, stiffness, and physical functioning of the joints.

    Full Information

    First Posted
    April 21, 2019
    Last Updated
    April 24, 2019
    Sponsor
    China Medical University Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03925467
    Brief Title
    Immediate Effects of Proximal and Distal Acupoints on the RPPW in Patients With KOA: a Randomized Controlled Trial
    Official Title
    Immediate Effects of Proximal and Distal Acupoints on the Radial Pressure Pulse-wave in Patients With Knee Osteoarthritis: a Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    April 30, 2019 (Anticipated)
    Primary Completion Date
    March 24, 2020 (Anticipated)
    Study Completion Date
    April 1, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    China Medical University Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Introduction: Knee osteoarthritis (KOA) is the most prevalent joint condition and is characterized by the progressive erosion of the articular cartilage. In TCM, Pulse Diagnosis has been one of the key diagnostic components in the clinical examinations. Modern pulse diagnosis studies have found that when the human body develops disease or is under pressure, the high frequency spectral energy (10-50Hz) will significantly change. Augmentation index (AIx) is related to the wave reflection of blood vessels. AIx can function as a useful index to reveal aging blood vessels. The experiment will use spectral energy and AIx as objective judgments about the efficacy of before-acupuncture and after-acupuncture treatment. Method: This randomized controlled study will recruit 120 participants which will be allocated to 3 groups: Distal Acupoints, Proximal Acupoints and Sham Acupoints. Each group will have 40 participants to ensure a sufficient sample size can be attained for statistical analysis. Participants aged 20 or older with acute or chronic arthritis will be recruited when they meet the Clinical Classification Criteria for KOA, that is knee pain and three out of six symptoms can be found in clinical practices, as recommended by the American College of Rheumatology:(a) any gender aged 50 years or above;(b) have less than 30 mins of morning stiffness ; (c) crepitus on active motion; and (d)bony tenderness;(e)bony enlargement; and (f)no palpable warmth.Objective and subjective baseline assessments and outcome evaluations including VAS, The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and range of knee motion will be performed. The primary outcome will be the assessment of Spectral Energy and AIx of radial pressure pulse-wave in both wrists (Chun, Guan, and Chy pulse) using the Pulse Sphygmograph before and after the intervention. The secondary outcome involves evaluating VAS and range of knee motion. Expected Outcome: The research findings can be clinical evidence regarding the effect of acupuncture KOA on radial artery. Moreover, the research will explore the immediate-effect difference between distal and proximal acupoints on KOA.
    Detailed Description
    Introduction: Knee osteoarthritis (KOA) is the most prevalent joint condition and is characterized by the progressive erosion of the articular cartilage. In TCM, Pulse Diagnosis has been one of the key diagnostic components in the clinical examinations. Modern pulse diagnosis studies have found that when the human body develops disease or is under pressure, the high frequency spectral energy (10-50Hz) will significantly change. Augmentation index (AIx) is related to the wave reflection of blood vessels. AIx can function as a useful index to reveal aging blood vessels. The experiment will use spectral energy and AIx as objective judgments about the efficacy of before-acupuncture and after-acupuncture treatment. Method: This randomized controlled study will recruit 120 participants which will be allocated to 3 groups: Distal Acupoints, Proximal Acupoints and Sham Acupoints. Each group will have 40 participants to ensure a sufficient sample size can be attained for statistical analysis. Participants aged 20 or older with acute or chronic arthritis will be recruited when they meet the Clinical Classification Criteria for KOA, that is knee pain and three out of six symptoms can be found in clinical practices, as recommended by the American College of Rheumatology:(a) any gender aged 50 years or above;(b) have less than 30 mins of morning stiffness ; (c) crepitus on active motion; and (d)bony tenderness;(e)bony enlargement; and (f)no palpable warmth.Objective and subjective baseline assessments and outcome evaluations including VAS, The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and range of knee motion will be performed. The primary outcome will be the assessment of Spectral Energy and AIx of radial pressure pulse-wave in both wrists (Chun, Guan, and Chy pulse) using the Pulse Sphygmograph before and after the intervention. The secondary outcome involves evaluating VAS and range of knee motion. Expected Outcome: The research findings can be clinical evidence regarding the effect of acupuncture KOA on radial artery. Moreover, the research will explore the immediate-effect difference between distal and proximal acupoints on KOA. Other Information: The study will be conducted in China Medical University Hospital(Meide Medical Building) Acupuncture Department and Yiyuantang Chinese Medicine Clinic, Hsinchu City. Under the acupuncture of a qualified Chinese physician who has had at least 10 years of clinical experience, it is expected that the risk to the subject will not exceed the minimum risk. The investigators will begin data collection as soon as the approval of the Research Ethics Committee and the required equipment are available, and is expected to be completed within one year of the IRB approval.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Knee Osteoarthritis
    Keywords
    knee osteoarthritis, acupuncture, radial pressure pulse-wave, spectral energy

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Three groups, pre-post intervention study
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    proximal acupoints
    Arm Type
    Experimental
    Arm Description
    Acupuncture needles will be administered at proximal acupoints
    Arm Title
    distal acupoints
    Arm Type
    Experimental
    Arm Description
    Acupuncture needles will be administered at distal acupoints
    Arm Title
    sham acupoints
    Arm Type
    Placebo Comparator
    Arm Description
    Sham acupuncture needles will be administered in the abdominal sham acupoints.
    Intervention Type
    Other
    Intervention Name(s)
    Acupuncture
    Intervention Description
    Proximal acupoints: disposable acupuncture needles will be inserted into acupoints (GB34, SP9, EX-LE2) bilaterally for a depth of 10-30 mm. Distal acupoints: disposable acupuncture needles will be inserted into acupoints (LI11, HT3, TE10) bilaterally for a depth of 10-30 mm. Sham acupoints: Sham acupuncture needles will be administered into sham acupoints RN12, ST21.
    Primary Outcome Measure Information:
    Title
    Assessment of Radial Pressure Pulse-wave at cunkou (1)
    Description
    Assessment of Radial Pressure Pulse-wave at cunkou ie at Cun, Guan & Chi of both hands before and after the intervention using Pulse Sphygmograph at 10 min before acupuncture.
    Time Frame
    20 min before acupuncture
    Title
    Assessment of Radial Pressure Pulse-wave at cunkou (2)
    Description
    Assessment of Radial Pressure Pulse-wave at cunkou ie at Cun, Guan & Chi of both hands before and after the intervention using Pulse Sphygmograph at 10 min after acupuncture.
    Time Frame
    10 min after acupuncture
    Secondary Outcome Measure Information:
    Title
    Range of knee motion
    Description
    Range of knee motion will be examined by a goniometer.
    Time Frame
    1) 10 min before acupuncture; 2) within 20 min after needle removal
    Title
    Visual analog scale (VAS)
    Description
    The intensity of pain is measure using VAS for pain. It is incorporated into the questionnaire with a scale of 0 (no pain) to 10 (worst pain possible)
    Time Frame
    1) within 40 min before acupuncture; 2) within 20 min after needle removal
    Title
    The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
    Description
    A questionnaire developed to evaluate the condition of patients with osteoarthritis of the knee and hip, including pain, stiffness, and physical functioning of the joints.
    Time Frame
    within 40 min before acupuncture

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients meet at least three out of the following six conditions: Any gender aged 50 years or above; Have less than 30 mins of morning stiffness; Crepitus on active motion; Bony tenderness; Bony enlargement; No palpable warmth. Exclusion Criteria: Subjects who are unable to walk. Malignancy, Any acute medical condition, Poorly controlled diabetes or hypertension, A motor or sensory nerve defect, Blood clotting disease, Mental illness, Dementia, Mental retardation or other abnormal person on the organic mind. Subjects with intra-articular solid or hyaluronic acid injection in the past 3 months. Knee surgery, Knee trauma, Congenital knee deformation, Severe knee varus or valgus deformation, Endocrine,metabolic, infectious, inflammatory, secondary degenerative knee arthritis caused by problems with rheumatic immune diseases. Subjects who are hypersensitive to needles. Subjects who are unwilling to cooperate or sign the subject consent.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Yu-Chen Lee, M.D.,PhD
    Phone
    886-975-682023
    Email
    d5167@mail.cmuh.org.tw
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Yu-Chen Lee, M.D.,PhD
    Organizational Affiliation
    China Medical University Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Immediate Effects of Proximal and Distal Acupoints on the RPPW in Patients With KOA: a Randomized Controlled Trial

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