CLINICAL TRIALS PROFILE FOR SUPRANE
All Clinical Trials for SUPRANE
| Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
|---|---|---|---|---|---|---|
| NCT00762372 ↗ | Japan Phase 2/3 Clinical Study With BLM-240 (Desflurane) | Completed | Baxter Healthcare Corporation | Phase 2/Phase 3 | 2008-02-01 | The purposes of this study are to evaluate the efficacy and safety of desflurane (BLM-240) as an anesthetic agent and to demonstrate the non-inferiority of desflurane to sevoflurane in term of awakening/recovery from anesthesia. |
| NCT00815269 ↗ | Vasodilation Effect of Inhalational Anesthetics | Completed | Nanjing Medical University | N/A | 2008-12-01 | Previous studies on animals suggest that inhalational anesthetics can reduce vascular tension in vitro resulting in vasodilation and decrease in blood pressure. This role for inhalational anesthetics has essential clinical implications such as the condition of sepsis or septic shock or other shock-associated states during which the blood vessel constricts strongly and leads to circulation dysfunction. The vasodilation property of these anesthetics including halothane, isoflurane, sevoflurane, desflurane and enflurane enables them to be better options than other general anesthetics in many clinical conditions needing the vasculature to be dilated. The investigators hypothesized that these inhalational anesthetics can evoke vasodilation measured with ultrasonography during general anesthesia in vivo as the in vitro studies displayed. |
| NCT01125982 ↗ | Postoperative Fatigue and Nausea Related to Choice of Anaesthetic Regimens | Completed | Sykehuset Telemark | Phase 4 | 2010-06-01 | The purpose of this study is to establish validated outcome measures for Postoperative Fatigue and Postoperative nausea, and to compare clinical impact of postanaesthetic symptoms during first week after Propofol or Desflurane based anaesthesia. |
| >Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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