Clinical Trials Directory

Trials / Completed

CompletedNCT00654511

Dexmedetomidine for Immediate Perioperative Analgesia in Pediatric Patients Undergoing Tonsillectomy

Dexmedetomidine for Immediate Perioperative Analgesia in Pediatric Patients Undergoing Tonsillectomy.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
101 (actual)
Sponsor
Children's National Research Institute · Academic / Other
Sex
All
Age
2 Years – 12 Years
Healthy volunteers
Accepted

Summary

The primary purpose of this study is: 1. To compare dexmedetomidine with fentanyl in terms of intra-operative hemodynamics and post-operative analgesia. 2. To determine an analgesic dose response relationship for dexmedetomidine. 3. Compare recovery characteristics of dexmedetomidine to fentanyl.

Conditions

Interventions

TypeNameDescription
DRUGFentanylFentanyl 1mcg/kg, Intravenous (IV)
DRUGFentanylFentanyl 2mcg/kg, Intravenous (IV)
DRUGDexmedetomidineDexmedetomidine, 2mcg/kg, Intravenous (IV)
DRUGDexmedetomidineDexmedetomidine, 4mcg/kg Intravenous (IV)

Timeline

Start date
2005-01-01
Primary completion
2008-10-01
Completion
2008-10-01
First posted
2008-04-08
Last updated
2021-03-23
Results posted
2011-04-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00654511. Inclusion in this directory is not an endorsement.