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
| Type | Name | Description |
|---|---|---|
| DRUG | S-ketamine | After 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. |
| DRUG | Placebo | After 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.