Clinical trials: Continuous IV Sedation
Mechanically Ventilated and Intubated Subjects
A Safety and Efficacy Study of Dexmedetomidine in ICU Patients Requiring Continuous Sedation
The purpose of this study is to evaluate the safety and efficacy of dexmedetomidine in ICU subjects who are initially intubated, mechanically ventilated and require sedation for beyond 24 hours.
- Trial name
- NCT00216190
- Testing
- Dexmedetomidine HCL Injection, Midazolam Injection
- Where
- 96 sites in United States, Argentina and 3 more
- Volunteers
- 420 people
- Sponsor
- Hospira, now a wholly owned subsidiary of Pfizer
Endotracheal Intubation, Continuous IV Sedation
Cerebral Perfusion Pressure Using Precedex and Other Sedatives
The purpose of this study is to examine the effects of using dexmedetomidine (Precedex) in addition to the current standard-of-care for sedation.
- Conditions
- Endotracheal Intubation, Continuous IV Sedation, ICP Monitoring
- Trial name
- C3PO (NCT01169467)
- Testing
- Standard-of-Care plus Dexmedetomidine, Standard-of-Care
- Where
- United States
- Volunteers
- 89 people
- Sponsor
- Duke University