Clinical Trial Results:
            Impact of a balanced infusion solution compound of 50% cristalloid and 50% colloid versus a unbalanced infusion solution of 100% cristalloid within a goal-directed hemodynamic protocol on acid-base balance in patients undergoing elective hip replacement surgery
Auswirkung der Anwendung einer balancierten Infusionslösungsmischung aus 50% kolloidaler und 50% kristalloider Lösung versus einer unbalancierten 100% kristalloiden Lösung innerhalb eines zielgerichteten Hämodynamik-Protokolls auf den Säure-Base Haushalt bei Patienten zur elektiven Hüfttotalendoprothese.
    
|     Summary | |
|     EudraCT number | 2009-016043-19 | 
|     Trial protocol | DE | 
|     Global completion date | 
                                    04 Nov 2011
                             | 
|     Paediatric regulatory details | |
|     Is the trial part of an agreed EMA paediatric investigation plan? | 
                                        No
                                 | 
|     Is the trial in scope of article 45 of Regulation (EC) No 1901/2006? | 
                                        No
                                 | 
|     Is the trial in scope of article 46 of Regulation (EC) No 1901/2006? | 
                                        No
                                 | 
|     Results information | |
|     Results version number | v1(current) | 
|     This version publication date | 
                                    03 Oct 2020
                             | 
|     First version publication date | 
                                    03 Oct 2020
                             | 
|     Other versions | |
|     Summary report(s) | link to publication | 
            Note: The legislation allows summary attachments to be posted instead of the full dataset for this trial. Refer to            Commission Guideline 2012/C 302/03
            for further information.    
 
				
