Acupuncture Therapy for Knee Osteoarthritis (ATKOA Ⅱ)
Knee Osteoarthritis
About this trial
This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Knee osteoarthritis, acupuncture, electroacupuncture, sham acupuncture
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
- NRS ≥ 4
Exclusion Criteria:
- Surgery history of knee or waiting for surgery (knee replacement or knee arthroscopy)
- Knee pain caused by other diseases (such as joint bodies, severe effusion of joint cavity, infection, malignant tumors, autoimmune diseases, trauma, fracture, gout, lumbosacral vertebrae disease, etc.)
- History of arthroscopy within 1 year or intra-articular injection within 4 months
- History of receiving acupuncture or massage treatment within 3 months
- Severe acute/chronic organic or mental diseases
- Coagulation disorders (such as hemophilia, etc.)
- Cardiac pacemaker, metal allergy or needle phobia
- Pregnant women, pregnant and lactating women
- Participation in another clinical study in the past 3 months
Sites / Locations
- Beijing Hostipal of Traditional Chinese Medicine affiliated to Capital medical University
- Guang'an Men Hospital, China Academy of Chinese Medical Sciences
- Beijing Hospital of Traditional Chinese and Western Medicine
- Dongfang Hospital Affiliated to Beijing University of Chinese Medicine
- Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine
- Hospital of acupuncture-Moxibustion, China Academy of Chinese Medical Sciences
- Beijing Friendship Hospital, Capital Medical University
- Affiliated Hospital of Hebei University of Chinese Medicine
- First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Sham Comparator
Electro-acupuncture
manual acupuncture
sham acupuncture
5 compulsory acupoints (ST35、EX-LE5、LR8、GB33 and Ashi) and 3 optional matching acupoints (stomach meridian syndrome:ST34、ST36、ST32、ST40、EX-LE2;gallbladder meridian syndrome:GB31、GB36、GB34、GB39、GB41;bladder meridian syndrome:BL39、BL40、BL57、BL60;San Yin meridian syndrome:LR7、SP9、SP10、KI10、SP4、SP6、LR3、KI3) will be chosen. Needles will be stimulated manually to achieve "De Qi" sensation and an electrical apparatus (Nanjing Jisheng Medical Co., Ltd., wave of 2/100Hz) will be then connected to the needles with alligator clips in pairs LR8-GB33 and two other matching acupoints. The stimulus intensity will be increased until the patient reports a strong but comfortable intensity. Patients will receive 30-minute, 24 sessions intervention over eight weeks.
Participants in the manual acupuncture 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.
Those in the sham acupuncture group receive shallow acupuncture at non-acupoints without manipulation,Deqi or actual current output.