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Clinical study on analgesic effect of dexmedetomidine combined with ropivacaine for femoral nerve block and early functional rehabilitation after total knee arthroplasty

Clinical study on analgesic effect of dexmedetomidine combined with ropivacaine for femoral nerve block and early functional rehabilitation after total knee arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071851
Enrollment
Unknown
Registered
2023-05-26
Start date
2022-10-22
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Total knee arthroplasty

Interventions

Experimental group 1:Femoral nerve block was performed with 0.1% ropivacaine 20ml after operation
Experimental group 2:Femoral nerve block was performed with 0.2% ropivacaine 20ml after operation
Experimental group 3:After operation, femoral nerve block was performed with 0.1% ropivacaine and dexmedetomidine 10µg, a total of 20ml
Experimental group 4:After operation, femoral nerve block was performed with 0.1% ropivacaine and dexmedetomidine 50µg, a total of 20ml?
Experimental group 5:After operation, femoral nerve block was performed with 0.1% ropivacaine and dexmedetomidine 100µg, a total of 20ml
Experimental group 6:Femoral nerve block was performed with 0.1% ropivacaine 20ml after operation

Sponsors

Gansu Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age: 40-75 years old; 2. Gender is not limited; 3.ASA classification I ~ II; 4. Implement total knee replacement; 5. Can communicate normally and have certain cognitive ability.

Exclusion criteria

Exclusion criteria: 1.Patients with coagulation dysfunction; 2. Patients infected with puncture site; 3. Patients with myopathy and severe liver and kidney diseases; 4. Patients with multiple trauma; 5. Patients with sensory or motor nerve damage of lower limbs caused by surgery or trauma in the past; 6. Those who are allergic to the drug used or any of its components or to similar drugs.

Design outcomes

Primary

MeasureTime frame
Pain score;Analgesia duration;

Secondary

MeasureTime frame
Temperature sense;Sense of touch;Activity score;First time to get out of bed;Patient satisfaction;Surgeon satisfaction;Length of stay;

Countries

China

Contacts

Public ContactYan Wenjun

Gansu Provincial Hospital

gsywj2008@hotmail.com+86 138 9337 0700

Outcome results

None listed

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