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The application of different dose dexmedetomidine in anesthesia of pediatric cardiac surgery

The application of different dose dexmedetomidine in anesthesia of pediatric cardiac surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017819
Enrollment
Unknown
Registered
2018-08-16
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

Congenital heart disease

Interventions

Dex low dose group:1µg/ml Dex
control group:saline
Dex high dose group:2µg/ml Dex

Sponsors

The Second Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 6 Years

Inclusion criteria

Inclusion criteria: 1. Patients with congenital heart disease (Ventricular septal defect, VSD,and atrioventricular septal defect, ASD). 2. Aged 1 year to 6 years old; 3. ASA I~III; 4. informed consent form from the parent or guardian.

Exclusion criteria

Exclusion criteria: 1. the patients who are not the first-time operation; 2. low birth weight or premature infant; 3. the patients who with serious cyanosis; 4. the patients who with brain paralysis; 5. the patients who with serious failure of respiratory, liver or renal fuction; 6. the patients who with metabolic dysfuction; 7. the patients who has been allergy with dex or high allergic people.

Design outcomes

Primary

MeasureTime frame
Hemodynamic index;Hemodynamic index;S-100ß;NSE;CK;CK-MB;H-FABP;H-FABP;Hs-TnT;BUN;Ccr;Cre;NGAL;

Countries

China

Contacts

Public ContactShaopeng Ming

Department of Anesthesology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China

495700284@qq.com+86 18076393856

Outcome results

None listed

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