Clinical Trials Directory

Trials / Completed

CompletedNCT05414006

Effect of S-ketamine in Cesarean Section Combined Anesthesia

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
120 (actual)
Sponsor
The Second Affiliated Hospital of Chongqing Medical University · Academic / Other
Sex
Female
Age
20 Years – 45 Years
Healthy volunteers
Not accepted

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

Conditions

Interventions

TypeNameDescription
DRUGS-ketamineS-ketamine or placebo were given to the fetus after delivery Patient-controlled intravenous analgesia or patient-controlled epidural analgesia were administered postoperatively

Timeline

Start date
2022-06-14
Primary completion
2022-08-31
Completion
2022-09-05
First posted
2022-06-10
Last updated
2023-02-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05414006. Inclusion in this directory is not an endorsement.