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Comparison of sevoflurane and propofol in the maintenance of of anesthesia of short term pediatric surgery with retention of spontaneous breathing: a randomized controlled trial

Comparison of sevoflurane and propofol in the maintenance of of anesthesia of short term pediatric surgery with retention of spontaneous breathing: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017396
Enrollment
Unknown
Registered
2018-07-28
Start date
2018-08-01
Completion date
Unknown
Last updated
2018-07-31

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

Conditions

anesthesia of short term pediatric surgery

Interventions

sevoflurane:Inhalation of sevoflurane
propofol:Intravenous infusion of propofol

Sponsors

Liaocheng People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 14 Years

Inclusion criteria

Inclusion criteria: The children's parents / guardians agreed to take part in the study; aged 0.5-12yr,weight 5-30kg,ASA status I-II;The children's ECG, chest radiograph, blood routine and blood biochemical examination before operation were normal; No cold, fever, diarrhea and other general anesthesia taboo, no allergic history of anaesthesia. The estimated operation time was within 60 min.

Exclusion criteria

Exclusion criteria: Children who are allergic to the study were excluded, who had upper respiratory tract infection, active airway disease and airway obstruction within two weeks before the test. Exclude cardiovascular, renal, lung, liver and brain (such as cerebral palsy, epilepsy, etc.) in children with abnormal function. Children with major systemic diseases, tumors, dyspnea, history of sleep apnea, developmental delay, mental, psychological and neurological diseases were excluded. Children who took any sedatives or painkillers with congenital metabolic defects within 2 weeks prior to the trial were excluded.Children who were overweight or obese were excluded from the normal weight of children in the corresponding age group.

Design outcomes

Primary

MeasureTime frame
the consumption of anesthetics;

Countries

China

Contacts

Public ContactGuisheng Wu

Liaocheng People's Hospital

wuguisheng001@163.com+86 133 4625 4197

Outcome results

None listed

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