Clinical Trials Directory

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

TypeNameDescription
DRUGKetamine Hcl 50Mg/Ml Injketamine infusion at a dose of 0.1 mg/kg/hour for 16 hours
DRUGKetamine Hcl 50Mg/Ml Injketamine infusion at a dose of 0.3 mg/kg/hour for 16 hours
OTHERControlWithout 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.