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A clinical study on the improvement of pain after total knee arthroplasty by auricular pressure and tendon manipulation

A clinical study on the improvement of pain after total knee arthroplasty by auricular pressure and tendon manipulation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000435
Enrollment
Unknown
Registered
2024-09-13
Start date
2024-09-02
Completion date
Unknown
Last updated
2024-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee arthritis

Interventions

Test group:Perioperative routine analgesia regimen+uricular pressure and tendon manipulation
Control group:Perioperative routine analgesia regimen

Sponsors

Department of Knee Joints Xi'an HongHui Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Overall physical condition is I-III according to the American College of Anesthesiologists (ASA) score; (2) Preoperative diagnosis of knee osteoarthritis mainly unilateral symptoms conservative treatment failed; (3) Unilateral TKA is planned; (4) Patients aged 50-80 years; (5) Those who are not allergic to the auricular point pressure bean in this study; (6) Be willing to provide written informed consent and participate in and comply with the study.

Exclusion criteria

Exclusion criteria: (1) Patients undergoing bilateral TKA unicondylar knee replacement or revision; (2) Patients with severe lesions in both knee joints; (3) Cardiovascular disease diabetes and perioperative blood glucose control was poor (fasting blood glucose > 8 mmol/L) severe Patients with severe renal insufficiency severe liver insufficiency history of gastric ulcer and coagulation disorders; (4) a history of stroke or neurological or psychiatric illness (serious mental illness psychological problems and inability to communicate); (5) Past drug addiction drug use history narcotic drug dependence drug abuse history and the use of hormone drugs treatment; (6) Patients who are allergic to the drug in this study and have pruritus and ulceration of the skin at the treatment site; Body mass index (BMI)>35kg/m2; (8) There is serious ligament instability; (9) Central and peripheral nervous system problems that cannot complete the postoperative rehabilitation program.

Design outcomes

Primary

MeasureTime frame
knee motion;Pain level;

Secondary

MeasureTime frame
Interleukin-6;Opioid use;C-reactive protein;

Countries

China

Contacts

Public ContactXiaobo Sun

Xi'an Honghui Hospital

1141839847@qq.com15735213367

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026