Overview
Analgesic Effect of Intraoperative Intravenous S-Ketamine After Total Knee Arthroplasty Surgery
Status:
Recruiting
Recruiting
Trial end date:
2024-03-01
2024-03-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Severe acute pain after total knee arthroplasty surgery has multiple implications for hospitals and patients, monopolising resources and affecting the quality of life. S-ketamine inhibits N-methyl-d-aspartate (NMDA) receptor activation and attenuates central sensitization associated with hyperalgesia, opioid tolerance.Therefore, the primary aim of this trial was to investigate whether s-ketamine decreases pain and opioid consumption postoperatively in adult individuals undergoing total knee arthroplasty surgery.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Qianfoshan HospitalTreatments:
Esketamine
Ketamine
Criteria
Inclusion Criteria:1. Patients understood the study in detail and voluntarily signed the informed consent
before the study;
2. Patients to be treated with total knee arthroplasty Surgery under General anesthesia;
3. Elderly patients(≥65y), regardless of gender; 4.18 kg/m2 ≤BMI≤30 kg/m2;
5.Patients can communicate normally; 6.Patients with ASA grade I-III; 7.Patients who have
no contraindications to drugs such as midazolam, fentanyl, s-ketamine.
Exclusion Criteria:
1. Increased intracranial or intraocular pressure;
2. severe hypertension;
3. unwillingness the study;
4. severe psychiatric disease and mental system diseases;
5. severe respiratory diseases;
6. hyperthyroidism;
7. liver and kidney dysfunction;
8. alcohol or drug abuse;
9. allergy to midazolam, fentanyl, s-ketamine.