Trials / Recruiting
RecruitingNCT06525584
Ketamine Infusion as a Method of Cerebral Protection in Children
Ketamine Infusion in the Postoperative Period as a Method of Cerebral Protection in Children During Surgical Correction of Congenital Heart Defects
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 196 (estimated)
- Sponsor
- Kemerovo State Medical University · Academic / Other
- Sex
- All
- Age
- 1 Month – 5 Years
- Healthy volunteers
- Not accepted
Summary
The study is devoted to the use of ketamine infusion in a subanesthetic dose in the postoperative period in children after surgical correction of congenital heart defects in children.
Detailed description
The study will examine the safety and effectiveness for neuroprotection of subanesthetic doses of ketamine in the postoperative period in children undergoing operations to correct septal congenital heart defects using cardiopulmonary bypass.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ketamine Hcl 50Mg/Ml Inj | ketamine infusion at a dose of 0.1 mg/kg/hour for 16 hours |
| DRUG | Ketamine Hcl 50Mg/Ml Inj | ketamine infusion at a dose of 0.3 mg/kg/hour for 16 hours |
| OTHER | Control | Without ketamine |
Timeline
- Start date
- 2023-11-05
- Primary completion
- 2025-12-01
- Completion
- 2025-12-01
- First posted
- 2024-07-29
- Last updated
- 2024-07-29
Locations
1 site across 1 country: Russia
Source: ClinicalTrials.gov record NCT06525584. Inclusion in this directory is not an endorsement.