Overview

Effect of S-ketamine in Cesarean Section Combined Anesthesia

Status:
Not yet recruiting
Trial end date:
2023-01-01
Target enrollment:
0
Participant gender:
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 perilactation
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
The Second Affiliated Hospital of Chongqing Medical University
Treatments:
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