Pediatric sedation
Conditions
Interventions
Control group:sufficient sedatives
Experimental group1:Sleep deprivation,sufficient sedatives
Experimental group2:Sleep deprivation+half dose sedatives
Sponsors
Guangdong Provincial People's Hospital(Guangdong Academy of Medical Sciences)
Eligibility
Sex/Gender
All
Age
No minimum to 4 Years
Inclusion criteria
Inclusion criteria: 1.Children aged 3 months to 4 years, regardless of sex;
Exclusion criteria
Exclusion criteria: 1.Chloral hydrate allergy; 2.Patients with severe hepatic/renal insufficiency, severe cardiac dysfunction, respiratory dysfunction, porphyria, gastritis, or being treated with anticoagulants. Children with obstructive sleep apnea syndrome; 3.Patients with diarrhea, rectal surgery, bloody stool, history of proctitis and colitis, and others who should not perform retention enema.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sedation failure rate with initial dose; | — |
Secondary
| Measure | Time frame |
|---|---|
| Imaging quality pass rate;Drug administration failure rate;Time elapsed until achieved sedation;Sedation failure rate after supplementation; | — |
Countries
China
Contacts
Public ContactXinyun Li
Guangdong Provincial People's Hospital(Guangdong Academy of Medical Sciences)
Outcome results
None listed