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
| Type | Name | Description |
|---|---|---|
| DRUG | Fentanyl | Fentanyl 1mcg/kg, Intravenous (IV) |
| DRUG | Fentanyl | Fentanyl 2mcg/kg, Intravenous (IV) |
| DRUG | Dexmedetomidine | Dexmedetomidine, 2mcg/kg, Intravenous (IV) |
| DRUG | Dexmedetomidine | Dexmedetomidine, 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.