Indications for all floating needles
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Knee obstruction: 1.Meets the diagnostic criteria for knee osteoarthritis in the "Guidelines for Diagnosis and Treatment of Osteoarthritis (2018 Edition)" developed by the Joint Surgery Group of the Chinese Medical Association's Orthopedic Branch; 2.Age: 50 to 75 years old, gender not limited; 3.During the first 2 weeks of enrollment, the average NRS score for knee joint pain was >= 4 points; 4.Disease grading, KOA imaging grading (Kellgren Lawrence, KL) 2-3 levels; 5.Agree to participate in this study, cooperate with the doctor to complete the study according to the research protocol, and sign the informed consent form. Only those who meet the above 5 criteria can be included in the study. Lumbago: 1.Meets the diagnostic criteria for back pain in the 2017 American Medical Association Guidelines for the Prevention and Treatment of Acute and Chronic Back Pain and the 2016 Chinese Expert Consensus on the Diagnosis and Treatment of Acute and Chronic Non Specific Back Pain; 2.Age range of 18 to 65 years old, without gender restrictions; 3.Cognitive correctness, able to correctly understand the relevant scales of clinical trials; 4.Agree to sign the informed consent form and voluntarily participate in this clinical study.
Exclusion criteria
Exclusion criteria: Knee obstruction: 1.Patients with severe cardiovascular, digestive, respiratory, urinary, hematopoietic and other diseases; 2.Knee joint pain caused by other diseases such as gouty arthritis, rheumatoid arthritis, knee joint deformities, etc; 3.The target knee joint has a history of surgery, intra-articular injection, or severe trauma within the past year; 4.Refusing to sign the informed consent form; 5.Received acupuncture and other treatments or took painkillers in the past month; 6.History of knee joint trauma and surgery within the past 6 months; 7.Previous history of neuromuscular related diseases, such as poliomyelitis; Lumbago: 1.Severe infection or damage to the acupoint area, affecting the operator; 2.Pain caused by stimulation or damage to nerve roots, as well as pain caused by fractures or injuries; 3.Merge with serious cardiovascular, renal, liver and other diseases that may affect the results of this clinical study (such as bone tuberculosis, tumors, severe osteoporosis, peripheral neuropathy, etc.); 4.Pregnant and lactating women, as well as those who have been ill and weak for a long time; 5.Those who are unable to cooperate with clinical research and provide accurate information on their condition to researchers, resulting in the inability to determine therapeutic efficacy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patient satisfaction;Data integrity;Data quality;System stable type; | — |
Countries
China
Contacts
Shandong Provincial Third Hospital