Clinical trial
Responsiveness to Noxious Stimuli in Ventilated Intensive Care Unit (ICU) Patients With Propofol / Remifentanil Sedation Protocol by Using the Nociception Flexion Reflex (RIII Reflex) and the Pupillary Dilatation Reflex.
NCT02916004 is registered in ClinicalTrials.gov with University Hospital, Antwerp as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Responsiveness to Noxious Stimuli in Ventilated Intensive Care Unit (ICU) Patients With Propofol / Remifentanil Sedation Protocol by Using the Nociception Flexion Reflex (RIII Reflex) and the Pupillary Dilatation Reflex.
- Lead sponsor
- University Hospital, Antwerp
- Phase
- Not applicable
- Overall status
- Completed
- Start date
- September 26, 2016
- Completion date
- July 14, 2018
- Enrollment
- 40 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.