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The efficacy of different concentrations of ropivacaine on ultrasound-guided ACB+ IPACK in total knee arthroplasty: a prospective, double-blind, randomized controlled trial

The efficacy of different concentrations of ropivacaine on ultrasound-guided ACB+ IPACK in total knee arthroplasty: a prospective, double-blind, randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049798
Enrollment
Unknown
Registered
2021-08-09
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

Osteoarthritis of the knee

Interventions

group A:The concentration of ropivacaine was 0.2% used for ACB+ IPACK
group B:The concentration of ropivacaine was 0.25% used for ACB+ IPACK
group C:The concentration of ropivacaine was 0.3% used for ACB+ IPACK

Sponsors

Anaesthetic surgery center, West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients requiring unilateral initial TKA surgery due to severe knee osteoarthritis; 2. Aged 40 to 80 years; 3. Body mass index 20~35 kg/m2; 4. The American Society of Anesthesiologists (ASA) classification (anesthesia risk assessment) is I ~ III level.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to anesthetics and sulfonamides; 2. There is moderate or higher knee joint deformity (varus and flexion) and joint stiffness; 3. Those who drink heavily or take opioids for a long time; 4. Language barriers and those who cannot complete the numerical rating scales (NRS) of pain; 5. Patients with neuropathy on the side of the operation; 6. Mental patients; 7. Those with previous peptic ulcer.

Design outcomes

Primary

MeasureTime frame
Postoperative dosage of remedial morphine hydrochloride;

Secondary

MeasureTime frame
Time to first postoperative analgesia;VAS pain score;Range of knee motion;Quadriceps strength;Time to first straight leg raise;The duration of hospital stay;Incidence of postoperative complications;

Countries

China

Contacts

Public ContactYang Jing

West China Hospital, Sichuan University

550298001@qq.com+86 18280213153

Outcome results

None listed

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