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A randomized controlled trial of two analgesic techniques on the recovery of motor function after total knee arthroplasty

A randomized controlled trial of two analgesic techniques on the recovery of motor function after total knee arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049032
Enrollment
Unknown
Registered
2021-07-20
Start date
2021-08-01
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

post-surgery of total knee arthroplasty

Interventions

CACB-IPACK group:CACB combined with IPACK
CACB-SNB group:CACB combined with SNB

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are going to undergo elective surgery for unilateral TKA; 2. Aged 18-80 years old; 3. ASA Class I-III; 4. BMI 18-40kg/m2.

Exclusion criteria

Exclusion criteria: 1. The patient refuses; 2. Infection at the puncture site; 3. Abnormal function of the lateral nerve to be blocked; 4. Patients who are allergic to the drugs used in this study (such as ropivacaine, flurbiprofen axetil, etc.); 5. Coagulation disorders; 6. Patients with severe liver and kidney dysfunction; 7. Patients with a history of mental illness or drug dependence.

Design outcomes

Primary

MeasureTime frame
First standing time after surgery;TUG test;

Secondary

MeasureTime frame
postoperative knee pain at rest and during movement within 48h;modified Bromage scores;ROM(range of motion);quadriceps muscle strength;patient satisfaction;length of hospital stay;incidence of postoperative complications;

Countries

China

Contacts

Public ContactZhu Caiyan

Shenzhen Second People's Hospital

c13823328449@163.com+86 13823328449

Outcome results

None listed

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