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Comparison of analgesia effectiveness of ultrasound-guided subsartorial fascial compartment block following total knee replacement

Comparison of analgesia effectiveness of ultrasound-guided adductor canal fascial compartment block following total knee replacement

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087587
Enrollment
Unknown
Registered
2024-07-30
Start date
2024-08-01
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Knee joint disease

Interventions

Adductor canal nerve vascular sheath inner compartment block group:Inject 20mL of 0.375% ropivacaine into the target area.
subsartorial fascial compartment of anterior part of the adductor canal block group:Inject 20mL of 0.375% ropivacaine into the target area.
Lateral fascial compartment of the adductor canal nerve vascular sheath block group:Inject 20mL of 0.375% ropivacaine into the target area.
Medial fascial compartment of the adductor canal nerve vascular sheath block group:Inject 20mL of 0.375% ropivacaine into the target area.
the vastus medialis and adductor muscles in the lateral and deep spaces of the neural vascular sheath:Inject 20mL of 0.375% ropivacaine into the target area.

Sponsors

Northern Jiangsu People's Hospital Affiliated to Yangzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Age (18-80 years old); Undergoing elective total knee arthroplasty, ASA classification I-III; Normal quadriceps strength preoperatively.

Exclusion criteria

Exclusion criteria: ASA classification IV; Prior motor and sensory dysfunction in the affected leg; Long-term use of opioid analgesics (>3 months); Allergy to local anesthetics; Infection at the puncture site; Coagulation dysfunction; Cognitive impairment, inability to communicate verbally; Patient unwilling to participate in this study.

Design outcomes

Primary

MeasureTime frame
pain numeric rating scale (0-10);

Secondary

MeasureTime frame
cumulative opioid consumption during the first 72 h;Number of cases requiring rescue analgesia during the first 72 hours postoperatively;Modified Bromage Scale;Knee Range of Motion;Patient Satisfaction;Sleep Quality;Postoperative Complications;pain numeric rating scale (0-10);pain numeric rating scale (0-10);spread distance of local anesthetic;hospitalization duration ;

Countries

China

Contacts

Public ContactCunjin Wang

Northern Jiangsu People's Hospital Affiliated to Yangzhou University

zebra1987@126.com+86 180 5106 1453

Outcome results

None listed

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