Sedation Clinical Trial
Official title:
Phase III Randomized Placebo-controlled Double Blind Comparative Study to Investigate the Efficacy and Safety of DA-9501 in Sedation During the Surgery With Epidural Anesthesia or Spinal Anesthesia Without Intubation Under Monitored Sedation Care
The purpose of this study is to examine the efficacy and safety of DA-9501 (Dexmedetomidine) in patients who require sedation during the surgery that requires epidural or spinal anesthesia without intubation under monitored sedation care.
Phase III, randomized, placebo controlled, double blind, parallel comparative study (Therapeutic confirmatory trial), to evaluate the efficacy and the safety of Dexmedetomidine in non-intubated patients who require sedation during surgery with spinal or epidural anesthesia under monitored sedation care ;
Status | Clinical Trial | Phase | |
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Recruiting |
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N/A | |
Completed |
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Recruiting |
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Recruiting |
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N/A | |
Recruiting |
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N/A | |
Completed |
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Phase 4 | |
Completed |
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N/A | |
Completed |
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Phase 1 | |
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N/A | |
Recruiting |
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Phase 3 | |
Active, not recruiting |
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N/A | |
Suspended |
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Cerebral Vascular Effects of Dexmedetomidine Versus Propofol Sedation in Intubated Mechanically Ventilated ICU Patients
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Phase 2/Phase 3 | |
Active, not recruiting |
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N/A | |
Completed |
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Phase 3 | |
Recruiting |
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Phase 4 | |
Completed |
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Phase 4 | |
Completed |
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Doxapram as an Additive to Propofol Sedation in Sedation for ERCP
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Phase 4 | |
Completed |
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Phase 4 | |
Completed |
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EUROpean Pain Audit In Neonates
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N/A |