Sunderby hospital
Luleå, 97180, Sweden
NCT Number: NCT03349593
Prevalence of biventricular function of the heart and preoperative level of venous return is not known in non-cardiac non-morbid obese population.
The aim of the study is to assess the preoperative function of the heart and status of hypovolemia on the day of surgery.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Luleå, 97180, Sweden
Preoperative transthoracic echocardiography (TTE) is conducted in 100 individuals. Biventricular function (i.e. systolic and diastolic properties), left ventricular filling pressures and level of venous return are assessed by TTE.
Moreover high-sensitive troponine I and Nt-proBNP, ECG are collected. Multiple echocardiographic parameters will be studied for feasibility in terms of preoperative assessment of the heart.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Preoperative transthoracic echocardiography
Time frame: One hour before surgery
Screening of preoperative level of venous return
Time frame: One hour before surgery
Screening of incidence of preoperative systolic and diastolic function
Umeå University
Other
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.
NCT06729268
Cardiovascular Diseases, Heart Diseases
Opole, Opole Voivodeship, Poland
View Trial DetailsNCT04202432
Cardiac Failure, Cardiovascular Diseases
Eindhoven, North Brabant, Netherlands
View Trial DetailsNCT04186416
Fluid Responsiveness, Hemorrhage
Paris, France
View Trial DetailsNCT05705115
Fluid Loss, Hemodynamic Instability
Oslo, Norway
View Trial Details