Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Edwards Lifesciences
The primary objective of this study is to evaluate the performance of the Acumen™ Assisted Fluid Management (AFM) Feature in its ability to predict a subject's fluid responsiveness.
Subjects enrolled in the validation study will have their fluid management decisions guided by the AFM Feature.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Be ≥ 18 years of age
Abdominal, pelvic, major peripheral vascular surgery expected to last \>2 hours post anesthesia induction
Participate or have authorized representative participate in the Informed Consent process and sign/date the IRB approved informed consent form.
You may not be if
Are \< 18 years of age
Emergent or cardiovascular surgical procedure
Are pregnant
Participation in any other drug, device, or biologic study concomitantly, or within the last 30 days (which may clinically interfere with this Clinical Study)
Refusal of patient or authorized representative to sign consent
Clareo Health | Assisted Fluid Management IDE Study
