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The application of nerve block in bilateral foot and ankle surgery

The application of nerve block in bilateral foot and ankle surgery: a randomized, controlled, double-blind study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053929
Enrollment
Unknown
Registered
2021-12-02
Start date
2021-12-15
Completion date
Unknown
Last updated
2022-10-31

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

Conditions

bilateral foot and ankle surgery

Interventions

Experimental group1:Left foot medication is 0.25% ropivacaine 30ml, right foot medication is 0.375% ropivacaine 30ml
Experimental group2:Left foot medication is 0.375% ropivacaine 30ml, right foot medication is 0.25% ropivacaine 30ml

Sponsors

Beijing Tongren Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 74 Years

Inclusion criteria

Inclusion criteria: 1. Patients with elective bilateral foot and ankle surgery; 2. Aged 18 to 74 years; 3. ASA I-III grade; 4. BMI (Body Mass Index) between 18-30Kg/m2; 5. Agree to participate in this study and sign the informed consent form before surgery.

Exclusion criteria

Exclusion criteria: 1. Anesthesia contraindications (coagulation disorders, infection at the puncture site, allergic to general or local anesthetics); 2. Predictably difficult airway; 3. Combined with central or peripheral neuropathy; 4. Pregnant women and lactating women; 5. Patients who use opioids for a long time; 6. Abnormal liver and kidney function: ALT and/or AST>2xULN, or TBIL>=1.5xULN; serum creatinine>112 µmol/L, or received dialysis treatment within 28 days before surgery; 7. Diabetic patients with unsatisfactory control of blood sugar (fasting blood sugar >= 11mmol/L during the screening period); 8. Participated in other clinical trials within 30 days; 9. Patients with combined tumor; 10. Charcot-type osteoarthropathy; 11. History of long-term use of hormones.

Design outcomes

Primary

MeasureTime frame
Time to first onset of pain after surgery;

Countries

China

Contacts

Public ContactWu Lili

Beijing Tongren Hospital Affiliated to Capital Medical University

trmzwulili@126.com+86 15201236168

Outcome results

None listed

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