Study identifier:0859IL/0068
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Multicenter, Comparative, Randomized Trial to Determine the Overall Safety and Efficacy of 1% Diprivan] vs 2% Diprivan vs Standard Agents Without Disodium Edetate for Sedation of Trauma, Postsurgical, or Critically Ill Pediatric Subjects.
sedation
N/A
-
-
-
-
Interventional
-
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2013 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|