Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01353378

Use of Dexmedetomidine in Children Undergoing Oral Maxillofacial Surgery to Decrease Emergence Delirium

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University · Academic / Other
Sex
All
Age
3 Years – 8 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine whether dexmedetomidine is effective in the treatment of emergence delirium of preschool children undergoing oral maxillofacial surgery.

Detailed description

Emergence delirium is a common side effect of sevoflurane anesthesia in children. Dexmedetomidine, because of its sedative and analgesic properties, might be useful for the management of this adverse effect. In the pediatric population, it has been shown to provide sedation for magnetic resonance imaging. Intravenously, it is has been shown to decrease emergence delirium following sevoflurane based anesthesia. The ability to administer a medication intravenously might solve the problem of emergence delirium and emergence agitation posed by the young patients undergoing oral maxillofacial surgery.

Conditions

Interventions

TypeNameDescription
DRUGdexmedetomidineIntravenously injecting 0.125microgram/kg for 10ml IV(in the vein)in group 1, 0.25microgram/kg for 10ml in group 2 within 10 minutes as soon as the operation begin. The control group receives 10mlsaline in 10 minutes.

Timeline

Start date
2011-06-01
Primary completion
2011-10-01
Completion
2011-12-01
First posted
2011-05-13
Last updated
2017-05-05

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01353378. Inclusion in this directory is not an endorsement.