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Efficacy of Electro-acupuncture Versus Manual Acupuncture on Knee Osteoarthritis

Primary Purpose

Osteoarthritis Of Knee

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Electro-acupuncture
Manual acupuncture
Sponsored by
zhouping
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis Of Knee

Eligibility Criteria

45 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 45-75 years old, male or female
  • Single / bilateral knee pain, duration of more than 6 months
  • KL (Kellgren-Lawrence) grade Ⅱ or Ⅲ
  • VAS ≥ 40mm
  • Signed informed consent

Exclusion Criteria:

  • Surgery history of knee or waiting for surgery (knee replacement or knee arthroscopy)
  • History of arthroscopy within 1 year or intra-articular injection within 4 months
  • Knee pain caused by other diseases (such as joint bodies, severe effusion of joint cavity, infection, malignant tumors, autoimmune diseases, trauma, etc.)
  • Severe acute/chronic organic or mental diseases
  • Coagulation disorders (such as hemophilia, etc.)
  • Pregnant women, pregnant and lactating women
  • History of receiving acupuncture or massage treatment within one month
  • Participation in another clinical study in the past 3 months
  • With a cardiac pacemaker, metal allergy or needle phobia

Sites / Locations

  • Beijing Hostipal of Traditional Chinese Medicine affiliated to Capital medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Electro-acupuncture group

Manual acupuncture group

Arm Description

After recruiting, patients are assigned to the electro-acupuncture group by randomization,and then receive electro-acupuncture treatment.Both treatments consist of 24 sessions of 30 minutes duration, administered over 8 weeks (usually three sessions per week). Participants in both groups will be evaluated at baseline, 4 weeks, 8 weeks, 12 weeks and 16 weeks.

After recruiting, patients are assigned to the manual acupuncture group by randomization,and then receive manual acupuncture treatment.Both treatments consist of 24 sessions of 30 minutes duration, administered over 8 weeks (usually three sessions per week). Participants in both groups will be evaluated at baseline, 4 weeks, 8 weeks, 12 weeks and 16 weeks.

Outcomes

Primary Outcome Measures

Success Rate
a change of 50% from baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain, stiffness and function scores at 8 weeks.

Secondary Outcome Measures

Pain
using WOMAC pain subscale
Stiffness
using WOMAC stiffness subscale
Knee-joint function
using WOMAC functional subscale
Quality of life
using the 12-Item Short Form Health Survey (SF-12)
Number of emergency analgesics (Celebrex/Loxonin) used
using Drug Use Form
Inflammatory markers
Luminex liquid chip method (LuminexxMAP, Technology, USA) Bio-plex200 system high throughput analysis platform (Bio-Rad) will be used to detect the expression of free protein in serum. Patients will receive fasting blood samples in the morning and then be centrifuged with 3000r/min, 15min in two hours.
Credibility/expectancy questionnaires
Credibility/expectancy questionnaires are used to assess the credibility and expectancy of the patients
Adverse events
using Adverse Event Form

Full Information

First Posted
August 30, 2017
Last Updated
September 5, 2017
Sponsor
zhouping
Collaborators
Beijing Friendship Hospital, Beijing Jishuitan Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03274713
Brief Title
Efficacy of Electro-acupuncture Versus Manual Acupuncture on Knee Osteoarthritis
Official Title
Efficacy of Electro-acupuncture Versus Manual Acupuncture for Knee Osteoarthritis: a Randomized Controlled Pilot Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 2017 (Anticipated)
Primary Completion Date
December 31, 2017 (Anticipated)
Study Completion Date
February 28, 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
zhouping
Collaborators
Beijing Friendship Hospital, Beijing Jishuitan Hospital

4. Oversight

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

5. Study Description

Brief Summary
Knee osteoarthritis (KOA), also called degenerative knee disease, is one of the most common bone and joint diseases in clinic. It often occurs in middle-aged people, especially women. It was estimated to affect more than 9 million individuals in the United States in 2005 and is a leading cause of disability and medical costs. Most elderly people over the age of 65 have radiographic and/or clinical evidence of osteoarthritis. KOA is a lifelong disease which can lead to obvious pain, joint stiffness, limitation of activity and even joint failure or disability.According to the papers published in the past years, we find that acupuncture therapy for the treatment of knee osteoarthritis include manual acupuncture, electro-acupuncture, acupotomy, laser acupuncture, fire needle and so on, among which manual acupuncture and electro-acupuncture are most commonly used.The aim of this study is to compare the effectiveness of electro-acupuncture and manual acupuncture in reducing pain and improving function in patients with KOA.
Detailed Description
Participants will be randomly allocated to one of two groups. Those in the first group receive electro-acupuncture, which involves having needles inserted into acupuncture points (locations on the body affected by acupuncture) which are stimulated manually for 10 seconds to create "De Qi" sensation and an electrical apparatus (HANS-200A acupoint nerve stimulator, Nanjing Jisheng Medical Co., Ltd. production, wave of 2/100Hz) was then connected to the needles with alligator clips to stimulate the needles in pairs ST36-SP9/GB34 and ST34-SP10. The stimulus intensity will be increased until the patient reported a strong but comfortable intensity. Those in the second group have the same schedule as the electro-acupuncture group except that the electrical apparatus has working power indicator and sound without actual current output. Both groups will receive 30-minute, 24 sessions intervention over eight weeks. Moreover, a number of questionnaires at the start of the study and then again after 4, 8, 12 and 16 week will be completed by participants. It is expected that participants will benefit from a decrease in pain and improved function. The risks of participation are minimal. Occasionally, acupuncture can make people feel nauseous or experience a temporary increase in pain either during or after treatment. Rare side effects during acupuncture treatment include fainting, infection and subcutaneous hematoma (pooling of blood under the skin). Participants will be warned of these potential side-effects before consenting to have acupuncture. Participants will be allowed, or required, to withdraw from the trial based on the following: A major protocol violation; Development of a serious disease preventing continuation in the trial; Adverse events related to acupuncture; Request to be withdrawn from the trial. The purpose is to accumulate clinical data, obtain the outcome data of the intervention method and prove the feasibility of the study protocol. Sixty patients will be selected as the sample size according to clinical experience.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis Of Knee

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Electro-acupuncture group
Arm Type
Experimental
Arm Description
After recruiting, patients are assigned to the electro-acupuncture group by randomization,and then receive electro-acupuncture treatment.Both treatments consist of 24 sessions of 30 minutes duration, administered over 8 weeks (usually three sessions per week). Participants in both groups will be evaluated at baseline, 4 weeks, 8 weeks, 12 weeks and 16 weeks.
Arm Title
Manual acupuncture group
Arm Type
Experimental
Arm Description
After recruiting, patients are assigned to the manual acupuncture group by randomization,and then receive manual acupuncture treatment.Both treatments consist of 24 sessions of 30 minutes duration, administered over 8 weeks (usually three sessions per week). Participants in both groups will be evaluated at baseline, 4 weeks, 8 weeks, 12 weeks and 16 weeks.
Intervention Type
Device
Intervention Name(s)
Electro-acupuncture
Intervention Description
Patients in this group will be treated by use of 6-7 local acupuncture points (ST34, ST35, ST36, EX-LE2, EX-LE5, GB33, GB34, SP9, SP10, LR7, LR8 and Ashi) and 2-3 distal points (GB31, GB36, GB39, GB41, ST40, ST41, LR3, BL60, SP6 and KI3). Needles will be stimulated manually for 10 seconds to achieve "De Qi" sensation and an electrical apparatus (HANS-200A acupoint nerve stimulator, Nanjing Jisheng Medical Co., Ltd. production, wave of 2/100Hz) will be then connected to the needles with alligator clips to stimulate the needles in pairs ST36-SP9/GB34 and ST34-SP10. The stimulus intensity will be increased until the patient reports a strong but comfortable intensity.
Intervention Type
Device
Intervention Name(s)
Manual acupuncture
Intervention Description
Participants in the group have the same schedule as the electro-acupuncture group except that the electrical apparatus has working power indicator and sound without actual current output.
Primary Outcome Measure Information:
Title
Success Rate
Description
a change of 50% from baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain, stiffness and function scores at 8 weeks.
Time Frame
baseline, 8 weeks
Secondary Outcome Measure Information:
Title
Pain
Description
using WOMAC pain subscale
Time Frame
baseline, 4 weeks, 8 weeks, 12 weeks and 16 weeks
Title
Stiffness
Description
using WOMAC stiffness subscale
Time Frame
baseline, 4 weeks, 8 weeks, 12 weeks and 16 weeks
Title
Knee-joint function
Description
using WOMAC functional subscale
Time Frame
baseline, 4 weeks, 8 weeks, 12 weeks and 16 weeks
Title
Quality of life
Description
using the 12-Item Short Form Health Survey (SF-12)
Time Frame
baseline, 4 weeks, 8 weeks, 12 weeks and 16 weeks
Title
Number of emergency analgesics (Celebrex/Loxonin) used
Description
using Drug Use Form
Time Frame
baseline, 4 weeks, 8 weeks, 12 weeks and 16 weeks
Title
Inflammatory markers
Description
Luminex liquid chip method (LuminexxMAP, Technology, USA) Bio-plex200 system high throughput analysis platform (Bio-Rad) will be used to detect the expression of free protein in serum. Patients will receive fasting blood samples in the morning and then be centrifuged with 3000r/min, 15min in two hours.
Time Frame
baseline, 8 weeks
Title
Credibility/expectancy questionnaires
Description
Credibility/expectancy questionnaires are used to assess the credibility and expectancy of the patients
Time Frame
baseline
Title
Adverse events
Description
using Adverse Event Form
Time Frame
up to 16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 45-75 years old, male or female Single / bilateral knee pain, duration of more than 6 months KL (Kellgren-Lawrence) grade Ⅱ or Ⅲ VAS ≥ 40mm Signed informed consent Exclusion Criteria: Surgery history of knee or waiting for surgery (knee replacement or knee arthroscopy) History of arthroscopy within 1 year or intra-articular injection within 4 months Knee pain caused by other diseases (such as joint bodies, severe effusion of joint cavity, infection, malignant tumors, autoimmune diseases, trauma, etc.) Severe acute/chronic organic or mental diseases Coagulation disorders (such as hemophilia, etc.) Pregnant women, pregnant and lactating women History of receiving acupuncture or massage treatment within one month Participation in another clinical study in the past 3 months With a cardiac pacemaker, metal allergy or needle phobia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cunzhi Liu, M.D
Phone
010-52176043
Email
lcz623780@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yongting Li, Postgraduate Student
Phone
15210518799
Email
liyong_ting@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cunzhi Liu, M.D
Organizational Affiliation
Beijing Hospital of Traditional Chinese Medicine
Official's Role
Study Director
Facility Information:
Facility Name
Beijing Hostipal of Traditional Chinese Medicine affiliated to Capital medical University
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100000
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32904642
Citation
Shi GX, Tu JF, Wang TQ, Yang JW, Wang LQ, Lin LL, Wang Y, Li YT, Liu CZ. Effect of Electro-Acupuncture (EA) and Manual Acupuncture (MA) on Markers of Inflammation in Knee Osteoarthritis. J Pain Res. 2020 Aug 26;13:2171-2179. doi: 10.2147/JPR.S256950. eCollection 2020.
Results Reference
derived
PubMed Identifier
32022581
Citation
Wang TQ, Li YT, Wang LQ, Shi GX, Tu JF, Yang JW, Hou YQ, Lin LL, Sun N, Zhao JJ, Hou HK, Liu CZ. Electroacupuncture versus manual acupuncture for knee osteoarthritis: a randomized controlled pilot trial. Acupunct Med. 2020 Oct;38(5):291-300. doi: 10.1177/0964528419900781. Epub 2020 Feb 5.
Results Reference
derived

Learn more about this trial

Efficacy of Electro-acupuncture Versus Manual Acupuncture on Knee Osteoarthritis

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