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A clinical study of the safety and efficacy of esketamine in patients undergoing pediatric congenital cardiac closure

A clinical study of the safety and efficacy of esketamine in patients undergoing pediatric congenital cardiac closure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096229
Enrollment
Unknown
Registered
2025-01-20
Start date
2025-01-25
Completion date
Unknown
Last updated
2025-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital heart disease

Interventions

Control group:General anesthesia induced fentanyl 2ug/kg+ propofol 2.5mg/kg
Experimental group:General anesthesia was induced with esketamine 1mg/kg.

Sponsors

Chinese People's Liberation Army Northern Theater Command General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1. Children with congenital heart disease undergoing interventional sealing under elective general anesthesia; 2. Age 1-10 years old; 3. American Society of Anesthesiologists (ASA) Grade II; 4. Patients or guardians fully understand the trial protocol and purpose and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Have a history of mental illness or symptoms of mental illness; 2. History of heart failure within the last 6 months; 3. Severe pulmonary hypertension (pulmonary systolic pressure >=70mmHg); 4. Liver and kidney insufficiency; 5. The experiment involved drug allergy; 6. Need muscular medication or mechanical ventilation.

Design outcomes

Primary

MeasureTime frame
Incidence of hypoxemia;

Secondary

MeasureTime frame
The number of respiratory depressions and the number of airway interventions given;

Countries

China

Contacts

Public ContactSun Yingjie

Chinese People's Liberation Army Northern Theater Command General Hospital

tansiqi2019@163.com+86 155 6617 8746

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026