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Effect of esketamine combined with ropivacaine on postoperative pain in patients with joint replacement

Effect of esketamine combined with ropivacaine on postoperative pain in patients with joint replacement

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065065
Enrollment
Unknown
Registered
2022-10-27
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

surgery patient

Interventions

Monotherapy group:Ropivacaine
Composite group:Esketamine combined with ropivacaine

Sponsors

The First People's Hospital of Lianyuangang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients must meet all of the following inclusion criteria to be included in this study: 1. 55 <= age <=75 years old, regardless of gender; 2. Elective knee replacement surgery; 3. ASA grade I or II; 4. 18 kg/m^2 < BMI<30kg/m^2; 5. Clearly understand and voluntarily participate in the study, and sign the informed consent form by himself/herself

Exclusion criteria

Exclusion criteria: Patients with any of the following were not eligible for this study: 1. Emergency surgery; hypovolemia, shock, or coma; 2. Planned spinal or epidural anaesthesia; 3. Infectious heart disease such as myocarditis or cardiac Endocarditis; sepsis; 4. Abnormal coagulation function (PT or INR >= 1.5*ULN, APTT >= 1.5*ULN); 5. Abnormal liver function, AST and/or ALT >= 2.5*ULN, TBIL >= 1.5*ULN; 6. Abnormal renal function, urea or urea nitrogen >= 1.5*ULN, serum creatinine greater than the upper limit of normal; 7. Acute heart failure; Unstable angina; myocardial infarction within 6 months before screening; resting ECG heart rate = 450 ms for males, >= 470 ms for females; 8. Hypertensive patients with unsatisfactory control of blood pressure (sitting systolic blood pressure >= 160 mmHg, and/or diastolic blood pressure >= 100 mmHg during screening); 9. Sitting systolic blood pressure = 11.1 mmol/L during screening); 11. Screening History of drug and/or alcohol abuse in the previous 2 years, which means drinking more than 2 units of alcohol per day on average (1 unit = 360 mL of beer or 45 mL of liquor with 40% alcohol content or 150 mL of wine); 12. Suffering from mental illness Systemic diseases (schizophrenia, mania, bipolar disorder, mental disorder, etc.) and long-term use of psychotropic drugs and cognitive dysfunction; 13. Esketamine, opioids, propofol, muscle relaxants Those who are allergic to or have contraindications to other drugs and their drug components; 14. Patients who are judged to be difficult to manage the respiratory tract (modified Markov score is grade IV); 15. Other situations that the investigator considers inappropriate to participate in this trial.

Design outcomes

Primary

MeasureTime frame
VAS;

Countries

China

Contacts

Public Contactchengzhi

The First People's Hospital of Lianyuangang

547694630@qq.com+86 18961321396

Outcome results

None listed

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