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Comparison of efficiency between the ultrasound-guided continuous adductor canal block and continuous femoral nerve block in the treatment of the pain after total knee arthroplasty

Comparison of efficiency between the ultrasound-guided continuous adductor canal block and continuous femoral nerve block in the treatment of the pain after total knee arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015045
Enrollment
Unknown
Registered
2018-03-03
Start date
2018-03-01
Completion date
Unknown
Last updated
2018-03-05

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

Conditions

pain after total knee arthroplasty

Interventions

Group A:ultrasound-guided continuous adductor canal block
Group F:ultrasound-guided continuous femoral nerve block

Sponsors

Foshan ChanCheng Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) undergone unilateral total knee arthroplasty; (2) aged 25-80 years old; (3) BMI 18-25 kg/m2; (4) ASA I-II.

Exclusion criteria

Exclusion criteria: (1) regional anesthesia contraindications (e.g. local infection); (2) having psychological problems or history of mental illness; (3) having serious cardiovascular disease, liver and kidney dysfunction or stroke; (4) allergy to local anesthetic or opioid drug; (5) having history of use of alcohol, drug abuse, opioids or town static drugs before operation; (6) having language difficulties or can not correctly understand the visual analog pain score; (7) having long-term use of opioids (3 months or daily use of opioids, almost every day); (8) having a limb neuropathology or history of lower extremity surgery or trauma and preoperative diabetes; (9) having peripheral neuropathy.

Design outcomes

Primary

MeasureTime frame
muscle strength of four biceps femoris at 8 h, 12 h, 24h, 72 h, 96 h, 120 h after surgery;Timed up and go test (TUG test) at 48h, 72 h, 96 h, 120 h after surgery;visual analogue scale (VAS) at 4 h, 6 h, 12 h, 24h, 72 h, 96 h, 120 h after surgery;The sensory block level of 4h, 6h, 8h, 12h, 24h, 48 h after operation;

Secondary

MeasureTime frame
Postoperative satisfaction at 4h, 6h, 8h, 12h, 24h, 48 h after operation;the rate of nausea and vomiting at 4h, 6h, 8h, 12h, 24h, 48 h after operation;the rate of retention of urine at 4h, 6h, 8h, 12h, 24h, 48 h after operation;the rate of tumble after operation;neural complications;Toxic reaction;

Countries

China

Contacts

Public ContactTaixin Chen

Foshan ChanCheng Center Hospital

chentaixin5401@dingtalk.com+86 18929985401

Outcome results

None listed

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