Fondazione Policlinico Universitario "A. Gemelli" IRCCS
Roma, 00168, Italy
NCT Number: NCT06439732
In this study investigators will study the association between the use of an hemodynamic monitoring system and the anesthetic consumption in patients following major abdominal surgery. Investigators will randomise patients for a control group and an intervention group. Patients belonging to intervention group will be monitored with a non-invasively continue system (Acumen IQ cuff sensor), while the control group will be monitored with a non-invasive intermittent pressure system. The total amount of mL of Sevoflurane will be registered in both groups and the difference will be considered as the aim of our study
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Roma, 00168, Italy
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Use of Acumen IQ cuff for haemodynamic monitoring
Time frame: During surgery
Time frame: during surgery
Time frame: during surgery
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Other
Acronym: HERMES
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07662577
Cardiovascular Diseases, Hypotension
Istanbul, Ataşehir, Turkey (Türkiye)
View Trial DetailsNCT05474027
Blood Loss, Surgical, Hemorrhage
Birmingham, Alabama, United States
View Trial DetailsNCT06950606
Hypotension During Surgery
Hamburg, Free and Hanseatic City of Hamburg, Germany
View Trial DetailsNCT07551219
Arrhythmias, Cardiac, Bradycardia
Ankara, Turkey (Türkiye)
View Trial Details