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A Centre-Randomized, Open-Label, Cross-Over Study to Compare the Pharmaco-Economic Consequences of an Ultiva (Remifentanil Hydrochloride) Based Regimen With Conventional Sedative Based Regimens in ICU Subjects Requiring Short-Term Mechanical Ventilation With Analgesia and Sedation

NCT00158873 Phase 4 COMPLETED

The study will evaluate the pharmaco-economic consequences of the use of a remifentanil based regimen compared with a conventional sedative based regimen in terms of duration of mechanical ventilation, length of stay in ICU, difference in extubation time and use of concomitant sedative agents.

Details

Lead sponsorGlaxoSmithKline
PhasePhase 4
StatusCOMPLETED
Enrolment224
Start date2004-09

Conditions

Interventions

Primary outcomes

Countries

Netherlands