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A clinical study of transcutaneous electrical acupoint stimulation combined with multi-modal analgesia in ERAS mode on improving pain and accelerating functional recovery after TKA

Not Applicable
Conditions
knee osteoarthritis
Registration Number
ITMCTR2200006633
Lead Sponsor
Wangjing Hospital of China Academy of Chinese Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

(1) Meet the diagnostic criteria of western medicine and traditional Chinese medicine for knee osteoarthritis, and the joint space is obviously narrowed on the weight-bearing frontal X-ray film, which is in line with Kellgren and Lawrence imaging grades III and IV, and is in line with unilateral total knee arthroplasty ( TKA) standard; patients with indications for surgery and ineffective after non-surgical treatment, patients and their families who are willing to undergo surgery.
(2) Aged 55-75 years old;
(3) The patient has normal intelligence, no language barrier, willing to receive treatment, and can cooperate with the doctor to successfully complete the postoperative pain grading score;
(4) The patient himself agrees and signs the consent form. effect, and its mechanism of effect in enhancing postoperative analgesic efficacy.

Exclusion Criteria

(1) Those who have a history of allergies to alcohol, morphine, non-steroidal anti-inflammatory drugs or local anesthetics;
(2) Those who have used sedatives, opioids for a long time, a history of alcohol abuse, and drug addicts;
(3) Postoperative patients Unstable vital signs, obvious high fever and chills, large fluctuations in blood pressure and heart rate;
(4) Neurosis and psychiatric patients;
(5) Postoperative prosthesis loosening, periprosthetic fracture, quadriceps tendon rupture, patellar tendon
(6) Those who are prone to bleeding and have severe heart, lung and renal insufficiency;
(7) Those who suffer from other rheumatism and metabolic diseases at the same time, such as gout, rheumatoid arthritis, Hemophilia, ankylosing spondylitis, etc;
(8) Those with electromagnetic devices in the body, such as cardiac pacemakers;
(9) Patients with purulent, non-specific knee joint infectious inflammation;
(10) At the same time Traumatic synovitis, villonodular pigmented synovitis and other patients with knee joint synovium as the main lesion.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual Analog Scale(VAS);Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC);
Secondary Outcome Measures
NameTimeMethod
Survival of life-12(SF-12);pain threshold;Pain Sensitization Assessment;Infrared thermal imaging;Opioid-related adverse reactions;Quadriceps motor unit potential duration and amplitude;ß-Endorphin(ß-EP);The dosage, frequency and time of use of drugs in the analgesic pump;
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