Clinical trial
Dexmedetomidine for Postoperative Sedation in Patients Undergoing Repair of…
NCT00409344 · Massachusetts General Hospital, Other · Terminated
Key facts
| NCT number | NCT00409344 |
|---|---|
| Title | Dexmedetomidine for Postoperative Sedation in Patients Undergoing Repair of Thoracoabdominal Aortic Aneurysms |
| Official title | Phase 4 Study of Dexmedetomidine for Postoperative Sedation in Patients Undergoing Repair of Thoracoabdominal Aortic Aneurysms |
| Lead sponsor | Massachusetts General Hospital, Other |
| Collaborators | Hospira, now a wholly owned subsidiary of Pfizer Industry |
| Status | Terminated |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Sedation, Respiration, Artificial, Length of Stay |
| Intervention type | Drug, Other |
| Interventions | Dexmedetomidine, Normal Saline |
| Enrollment | 0 |
| Start date | Jan 1, 2007 |
| Primary completion | Jan 1, 2008 |
| Completion | Jan 1, 2008 |
| First posted | Dec 8, 2006 |
| Last update posted | Sep 22, 2009 |
| Countries | United States |
At a glance
- 1–9 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: