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Randomized Controlled Trial on Transcutaneous Electrical Acupoints Stimulation For Acute Pain After Total Knee Arthroplasty

Randomized Controlled Trial on Transcutaneous Electrical Acupoints Stimulation For Acute Pain After Total Knee Arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016347
Enrollment
Unknown
Registered
2018-05-26
Start date
2018-05-31
Completion date
Unknown
Last updated
2018-05-28

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

Conditions

osteoarthritis

Interventions

5Hz TENS:Two circular electrodes of TENS are placed on the points surrounding the knee, Yinglingquan and Yanglinguqan, respectively. The TENS unit generates a balanced, asymmetric, bidirectional wavef
100Hz TENS:Two circular electrodes of TENS are placed on the points surrounding the knee, Yinglingquan and Yanglinguqan, respectively. The TENS unit generates a balanced, asymmetric, bidirectional wav
mixed TENS:Two circular electrodes of TENS are placed on the points surrounding the knee, Yinglingquan and Yanglinguqan, respectively. The TENS unit generates a balanced, asymmetric, bidirectional wav
placebo TENS:The placebo TENS unit applied TENS at 100 Hz, 200 ls for 30 s and then the current ramped off over a 15-s time frame. Intensity was turned up until the subject reported feeling the stimul

Sponsors

School of rehabilitation medicine, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Age 50-80 years old; (2) BMI <25kg/m2; (3) diagnosis of knee osteoarthritis; (4) primary unilateral total knee arthroplasty; (5) The surgical procedure is consistent; (6) The American Association of Anesthesiologists (ASA) I-II; (7) The anesthetic methods are standard general anesthesia.

Exclusion criteria

Exclusion criteria: (1) People with hyposensory or sensory impairment (acupuncture sensation in the lower extremities of the affected side with = 5 skin areas disappeared); (2) preoperative opioid intake (normal use of drugs more than 2 weeks before surgery within 6 months); (3) TENS therapy or other therapeutic methods that affect the therapeutic efficacy of pain within 2 weeks; (4) Those who have contraindications to TENS, such as pacemakers or those who are allergic to nickel; (5) It is unable to maintain its own walking safety without the support of auxiliary equipment; (6) Patients with severe cardio-cerebral vascular disease, liver, kidney and hematopoietic system diseases or organ failure, mental illness, etc. cannot be tolerated.

Design outcomes

Primary

MeasureTime frame
Numerical rating scale;Numerical rating scale;knee society score;

Secondary

MeasureTime frame
active range of motion of knee;surface electromyography of quadriceps;modified 30s sit to stand test;modified 30s sit to stand test;Additional use of analgesics;SF-36;

Countries

China

Contacts

Public ContactLi Yulin

School of rehabilitation medicine, Shanghai University of Traditional Chinese Medicine

18817775630@163.com+86 18817775630

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 3, 2026