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Comparison of application of ropivacaine combined with different concentrations of dexmedetomidine in nerve block in orthopedic foot and ankle surgery

Comparison of application of ropivacaine combined with different concentrations of dexmedetomidine in nerve block in orthopedic foot and ankle surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048474
Enrollment
Unknown
Registered
2021-07-09
Start date
2021-08-01
Completion date
Unknown
Last updated
2022-03-21

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

Conditions

None listed

Interventions

Group A:0.375% ropivacaine 30ml
Group B:0.375% ropivacaine + 0.25ug/kg dexamethasone 30ml
Group C:0.375% ropivacaine + 0.5ug/kg dexamethasone 30ml
Group D:0.375% ropivacaine + 0.75ug/kg dexamethasone 30ml
Group E:0.375% ropivacaine + 1ug/kg dextromethorphan 30ml

Sponsors

Tongren Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years, planning to undergo elective foot and ankle surgery under general anesthesia in Beijing Tongren Hospital; 2. ASA level 1-3; 3. Single foot surgery, the estimated operation time is 0-3 hours; 4. BMI 18-30 kg/m^2; 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
first pain time;time to first request analgesia;

Secondary

MeasureTime frame
pain score;adverse effect( itch, dizzy,nausa,consciousness, retention of urine);analgesic need in 24 and 48h;overall satisfaction;adverse effects of nerve block;

Countries

China

Contacts

Public ContactWang Guyan

Beijng Tongren Hospital

guyanwang2006@163.com+86 13910985139

Outcome results

None listed

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