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Weaning of Norepinephrine Guided by the Dynamic Arterial Compliance in Cardiac Surgery Post Operative.

Weaning of Norepinephrine Guided by the Dynamic Arterial Compliance in Cardiac Surgery Post Operative.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02479529
Acronym
SNEAD
Enrollment
130
Registered
2015-06-24
Start date
2014-10-31
Completion date
2016-06-30
Last updated
2025-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vasoplegic Syndrome

Brief summary

After cardiac surgery, vasoplegic syndrome is a hemodynamic state characterized by profound hypotension associated with a decrease in systemic vascular resistance. The care of this disease is based on the intravenous administration of a vasopressor, usually norepinephrine. During the recovery phase, weaning of norepinephrine, is an important step in which any lack of preload (blood volume) initial or secondary can be, and increase tissue malperfusion.

Interventions

DRUGNorepinephrine

Administration and weaning of norepinephrine is based on dynamic arterial elastance

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Major patient ≥ 18 years * Patient operated a cardiac surgery for myocardial revascularization (CABG surgery) or surgical correction of valvular or combined surgery (CABG and valve disease) or surgery the ascending aorta and cardiac surgery with vasoplegic syndrome treated by norepinephrine * Signed consent * Affiliation to social assurance

Exclusion criteria

* Permanent atrial fibrillation * Treatment with dobutamine and/or epinephrine * Pregnant woman * Patient under guardianship or private public law * Internal pacemaker * Hypothermia * Patient refusal

Design outcomes

Primary

MeasureTime frameDescription
The duration of treatment with norepinephrine.Day 28Mean duration time of norepinephrine administration calculated in hours

Secondary

MeasureTime frameDescription
ICU duration of stay in dayDay 28
Total urine output in ml during the study periodDay 28
Total of crystalloid an colloid infused during the study period (ml)Day 28
The total dose of norepinephrine infused during the study periodDay 28
Incidence of postoperative atrial arrhythmias (Ac/Fa, Ventricular tachycardia, Ventricular flutter, Ventricular fibrillation) during the study periodDay 28
SOFA scoreDay 28SOFA score measured at the end of norepinephrine administration
the rate of arterial lactate at the end of norepinephrine administrationDay 28

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026