Clinical Trials Directory

Trials / Unknown

UnknownNCT05299866

The Effect of S-ketamine Combined With Sufentanil for Postoperative Analgesia in Patients Following Cesarean Section

The Effect of Low-dose of S-ketamine Combined With Sufentanil for Postoperative Patient-controlled Intravenous Analgesia in Patients Following Cesarean Section

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
216 (estimated)
Sponsor
Ling Dong · Academic / Other
Sex
Female
Age
20 Years – 40 Years
Healthy volunteers
Not accepted

Summary

This randomized controlled trial is designed to investigate the effect of low-dose of S-ketamine combined with sufentanil for postoperative patient-controlled intravenous analgesia in patients following cesarean section.

Conditions

Interventions

TypeNameDescription
DRUGS-ketamineAfter surgery, patient-controlled analgesia is provided. The pump is established with S-ketamine 1mg/kg, sufentanil 2microgram/kg, andondansetron16mg, diluted with normal saline to 100 ml. The pump is programmed to deliver 2 ml boluses with a background infusion rate at 2 ml /h and a 30 min lockout interval.
DRUGPlaceboAfter surgery, patient-controlled analgesia is provided. The pump is established with sufentanil 2microgram/kg, andondansetron16mg, diluted with normal saline to 100 ml. The pump is programmed to deliver 2 ml boluses with a background infusion rate at 2 ml /h and a 30 min lockout interval.

Timeline

Start date
2022-04-12
Primary completion
2024-05-31
Completion
2024-06-30
First posted
2022-03-29
Last updated
2023-02-28

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05299866. Inclusion in this directory is not an endorsement.