Overview
Effect of S-ketamine in Cesarean Section Combined Anesthesia
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2023-01-01
2023-01-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
To compare the anti-hyperalgesia effect between S-ketamine with placebo for Maternal receiving elective Cesarean Section under Combined spinal and epidural analgesia. Based on this study the investigators intend to verify the role and potential mechanism of S-ketamine combined anesthesia in alleviating hyperalgesia after cesarean section, prove that it can reduce hyperalgesia and postoperative pain. explore the role of S-ketamine in alleviating postoperative hyperalgesia in different PCA ways and explore the safety of S-ketamine in the perilactationPhase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
The Second Affiliated Hospital of Chongqing Medical UniversityTreatments:
Esketamine
Ketamine
Criteria
Inclusion Criteria:- ASA status I-III
- Age 20 to 45
- 37-42 weeks gestation
- undergo elective cesarean section with subarachnoid anesthesia
- participate in this study and sign informed consent
Exclusion Criteria:
- Patients with contraindications for cesarean section
- Patients with contraindications of combined spinal and epidural anesthesia
- Patients with severe systemic disease
- Alcoholism and long-term use of anti-inflammatory and analgesic drugs
- Patients who were unable to cooperate or refused to participate in the trial
- Patients with contraindications to esketamine and hydromorphone