Skip to content

Study on the brain central mechanism of opposing needling analgesia after total knee arthroplasty based on multimodal MRI

Study on the brain central mechanism of analgesic effect of opposing needling on total knee arthroplasty based on resting BOLD-fMRI

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042429
Enrollment
Unknown
Registered
2021-01-21
Start date
2021-01-22
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Pain after knee arthroplasty

Interventions

Sponsors

Guanghua Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) 50 to 75 years of age. (2) Osteoarthritis of knee joint was diagnosed and unilateral total knee arthroplasty was performed under general anesthesia in hospital. no surgical contraindications, and agreed to participate in this trial. (3) the American Association of Anesthesiologists (ASA) is classified as I or II. (4) all the affected limbs were right knee. (5) all of them are right-handed. (6) consent and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) There was deep venous thrombosis or swelling of lower extremities before operation. (2) Severe arrhythmias, heart failure, chronic obstructive pulmonary disease, epilepsy, mental illness. (3) Patients with brain injury were found after baseline fMRI examination. (4) There were obvious mood swings within 24 hours before fMRI scan. (5) Drinking alcohol, coffee, strong tea, etc., within 24 hours before fMRI scan. (6) During fMRI scan, severe structural or deterministic injuries were found on both sides of the skull. (7) If acute or serious events or adverse events occur during the study, they should not continue to participate in the trial. (8) Patients who received other related treatments on their own during the trial. (9) Poor compliance, repeated explanations are still unwilling to participate in the test, or unable to complete the test cycle.

Design outcomes

Primary

MeasureTime frame
Resting state BOLD-fMRI detection index: low frequency amplitude (ALFF), fractional low frequency amplitude (f ALFF), local consistency analysis (ReHo), functional connection (FC).;Pressure pain threshold;

Secondary

MeasureTime frame
Visual analogue score (VAS) (includes pain during rest and activity);4m walking test;

Countries

China

Contacts

Public ContactXiao Lianbo

Guanghua Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine

xiao_lianbo@163.com+86 13849429347

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026