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The effect of the IPACK block on pain after primary TKA in different levels of knee flexion deformity patients: a prospective, cohort trial

The effect of the IPACK block on pain after primary TKA in different levels of knee flexion deformity patients: a prospective, cohort trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035146
Enrollment
Unknown
Registered
2020-08-02
Start date
2020-08-01
Completion date
Unknown
Last updated
2020-08-03

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

Conditions

knee osteoarthritis/ knee rheumatoid arthritis

Interventions

The knee flexion deformities of different degrees were divided into different groups, and the patients without knee flexion deformity were the control group:Under the guidance of ultrasound, 20 ml 0.2

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Eligible patients will be those scheduled for an elective unilateral, primary TKA, aged 18 to 80 years, and American Society of Anesthesiologists Physical Status classification I-III.

Exclusion criteria

Exclusion criteria: Contraindication to regional anesthesia or peripheral nerve blocks, allergy to local anesthetics, allergy to nonsteroidal anti-inflammatory drugs (NSAIDs), chronic renal insufficiency (Cr > 1.4 mg/dL or glomerular filtration rate 3 months), pre-existing peripheral neuropathy involving the operative site, and body mass index > 40 kg/m2.

Design outcomes

Secondary

MeasureTime frame
baseline characteristics of patients (age,gender, weight, height, surgery side, VAS pain score, Knee range of motion, quadriceps strength, ASA status, duration of operation;haematological indicators (CRP, IL-6, fasting blood-glucose);visual analogue scale pain score and rescue analgesia;postoperative functional recovery(degree of knee range of motion, quadriceps strength, daily mobilization);postoperative adverse events;

Countries

China

Contacts

Public ContactZongke Zhou

West China Hospital, Sichuan University

zhouzongke@scu.edu.cn+86 18980601028

Outcome results

None listed

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