WHO ICTRP trial
Dexmedetomidine combined with propofol intravenous sedation in outpatient…
ChiCTR2000033541 · Chinese Clinical Trial Registry (ChiCTR) · Not Recruiting
Key facts
| Trial ID | ChiCTR2000033541 |
|---|---|
| Public title | Dexmedetomidine combined with propofol intravenous sedation in outpatient imaging in children: a randomized controlled clinical study |
| Scientific title | Dexmedetomidine combined with propofol intravenous sedation in outpatient imaging in children: a randomized controlled clinical study |
| Primary sponsor | Guangzhou Women and Children Medical Center |
| Registry | Chinese Clinical Trial Registry (ChiCTR) |
| Recruitment status | Not Recruiting |
| Study type | Interventional study |
| Phase | 4 |
| Countries | China |
| Conditions | Outpatient sedation in children |
| Interventions | Group Chloral hydrate:Oral take 10% chloral hydrate by 0.5ml/kg sedation;Group Propofol:Propofol iv sedation;Group Dex & Pro:Dex&Pro iv sedation |
| Registration date | Jun 4, 2020 |
| Target size | Group Chloral hydrate:120;Group Propofol:120;Group Dex & Pro:120 |
| Registry page | chictr.org.cn |
At a glance
- No Results available
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: