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Dexmedetomidine Versus Propofol for Cerebral Angiography in Pediatric Patients

Dexmedetomidine Versus Propofol for Cerebral Angiography in Pediatric Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002713
Enrollment
Unknown
Registered
2012-10-23
Start date
2011-03-19
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

pediatric cerebrovascular disease

Interventions

dexmedetomidine group:dexmedetomidine
propofol group:propofol

Sponsors

Department of Anesthesiology, First Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
6 Years to 15 Years

Inclusion criteria

Inclusion criteria: Children between the ages of 3 and 15 years with ASA classification17 of I or II were eligible for inclusion in the study.

Exclusion criteria

Exclusion criteria: Exclusion criteria were known allergy to a-2 agonists, obesity, ASA classification III or more, cardiac abnormalities, craniofacial anomaly, respiratory problems (pneumonia, asthma, bronchitis and severe obstructive sleep apnea), Glasgow Coma Scale (GCS)<15, intracranial hypertension and uncontrolled epilepsy.

Design outcomes

Primary

MeasureTime frame
hemodynamic changes;adverse event;

Countries

China

Contacts

Public ContactKe Peng
pengke0422@163.com+86 15962155989

Outcome results

None listed

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