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Application of Fascia Iliaca Compartment Block Combined with Infiltration between the Popliteal Artery and Capsule of the Knee for Postoperative Analgesia after Total Knee Arthroplasty

Application of Fascia Iliaca Compartment Block Combined with Infiltration between the Popliteal Artery and Capsule of the Knee for Postoperative Analgesia after Total Knee Arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117149
Enrollment
Unknown
Registered
2026-01-20
Start date
2025-02-06
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Postoperative analgesia after total knee arthroplasty

Interventions

Experimental group:Infiltration between the popliteal artery and capsule of the kneeon on the basis of fascia iliaca block

Sponsors

Zibo Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 50 to 80 years old; 2. Scheduled for primary unilateral total knee arthroplasty; 3. Diagnosed with primary knee osteoarthritis (Kellgren-Lawrence grade ?-?) by imaging and clinical examination; 4. American Society of Anesthesiologists (ASA) physical status classification ?-?; 5. Conscious, with good communication skills, able to understand the research content and cooperate in completing the evaluation; 6. Voluntarily participate and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with hypersensitivity to local anesthetics; 2. Patients with coagulation disorders (platelet count 1.5); 3. Patients with severe cardiac, pulmonary, hepatic, or renal dysfunction (NYHA class ?–? cardiac function, forced expiratory volume in one second (FEV1) < 50% of predicted value, Child-Pugh class C liver function, or estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73m^2); 4. Patients with a history of mental illness or cognitive impairment who are unable to cooperate with the evaluation; 5. Patients with a previous history of ipsilateral knee joint surgery; 6. Pregnant or lactating women; 7. Patients who refuse to participate in this study or are unable to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale;

Secondary

MeasureTime frame
Proportion of patients with active knee flexion angle >= 90° within 24 hours after surgery;Proportion of patients able to walk >= 10 meters with assistance within 48 hours after surgery;Postoperative muscle strength of the quadriceps, ankle dorsiflexors, and ankle plantar flexors;Patient satisfaction score;Adverse reactions within 48 hours after surgery;

Countries

China

Contacts

Public ContactLi Yubao

Zibo Traditional Chinese Medicine Hospital

zibolyb@163.com+86 185 6039 5821

Outcome results

None listed

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