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The study for ultrasound -guided adductor canal block for postoperative analgesia after total knee arthroplasty

The study for ultrasound -guided adductor canal block for postoperative analgesia after total knee arthroplasty

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019468
Enrollment
Unknown
Registered
2018-11-12
Start date
2018-11-21
Completion date
Unknown
Last updated
2018-11-19

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

Conditions

Pain

Interventions

A:ultrasound -guided adductor canal block
B:local anesthetic infiltration

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) aged 50 to 80 years; 2) total knee replacement under general anesthesia; 3) American society of anesthesiologists (ASA) grade I - II; 4) be able to communicate well with researchers and comply with the whole test requirements; 5) understand the purpose of the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1) known allergy to any of the drugs or components in the program; 2) infection of the puncture site; 3) communication disorder or failure to cooperate; 4) clear past existence of cognitive impairment or mental illness (see Table 2); 5) secondary operation; 6) preoperative VAS score = 4 and lasting more than 2 weeks; 7) patients with liver and kidney dysfunction; 8) patients with peripheral neuropathy (such as diabetes mellitus, Lyme disease, uremia, porphyrin disease, Guillain-Barre syndrome) and peripheral nerve injury of lower extremity; 9) long term history of hormone use, history of chronic bronchitis, history of asthma, recent pulmonary infection; 10) chronic alcoholics (who have not been sober in the last three months); 11) to participate in other clinical trials in the last three months; 12) to have a blood coagulation disorder or haemorrhagic disease; 13) to be allergic to ultrasound coupling agents.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale/Score;Muscle strength grading;

Countries

China

Contacts

Public ContactHailian Wang

Huashan Hospital, Fudan University

wang-hai-lian@hotmail.com+86 13661672208

Outcome results

None listed

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