Last updated: 11/07/2018 19:49:03
An economic evaluation of an analgesia-based sedation regimen with remifentanil supplemented with propofol compared to a conventional sedation regimen with midazolam/fentanyl in the ICU for patients after cardiac surgery
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
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Trial status
Study complete
Study complete
Trial overview
Official title: An economic evaluation of an analgesia-based sedation regimen with remifentanil supplemented with propofol compared to a conventional sedation regimen with midazolam/fentanyl in the ICU for patients after cardiac surgery
Trial description: An economic evaluation of an analgesia-based sedation regimen with remifentanil supplemented with propofol compared to a conventional sedation regimen with midazolam/fentanyl in the ICU for patients after cardiac surgery
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Muellejans B, Matthey T, Schlopp J et al., Sedation in the intensive care unit with remifentanil/propofol versus midazolam/fentanyl: a randomised, open-label pharmacoeconomic trial. Critical Care 2006, 10:R91
Medical condition
Anaesthesia
Product
remifentanil
Collaborators
Not applicable
Study date(s)
November 2001 to Invalid Date
Type
Not applicable
Phase
4
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
Not applicable
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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