Lactated Ringer's Versus 5% Human Albumin: Cardiac Surgical Patients

Stopped early · Phase 2

Conditions studied: Hemodynamic Stability

In brief

The purpose of this study is to show which of two different types of fluid is best for cardiac surgical patients. During and after the subject's heart surgery, the subject will be given either Lactated Ringer's or 5% human albumin to replace lost blood and body fluids and to regulate blood pressure. Albumin (human) 5% is a sterile, liquid preparation of albumin derived from large pools of human plasma. All units of human plasma used in the manufacture of Albumin (human) 5% are provided by FDA approved blood establishments only. Lactated Ringer's is a sterile, nonpyrogenic solution containing isotonic concentrations of electrolytes in water for injection. It is FDA approved for administration by intravenous infusion for parental replacement of extracellular losses of fluid and electrolytes. The hypothesis of this study is that the individual total fluid volume and alveolar-arterial gradient will be less with 5% human albumin compared to Lactated Ringer's in the perioperative cardiac surgical patient.

Key facts

Study ID

NCT02654782

Run by

William C. Oliver

People needed

10

Starts

2016-01-01

Expected to finish

2017-10-09

Last updated by the study team

2019-04-16

Who can join

Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Non-pregnant female patients
• Patients undergoing elective cardiac surgery
• Aspirin, heparin, or warfarin preoperatively accepted

You may not qualify if…

• Previous sternotomy
• Emergency surgery
• Combined procedures (vascular or thoracic operations)
• Congenital heart repair
• Hypothermic cardiopulmonary bypass (CPB) < 28 degrees C
• Serum creatinine greater than or equal to 1.5 mg/dL
• Dialysis dependent renal failure
• Neurologic injury or event within 30 days (including transient ischemic attack)
• Cerebrovascular accident with significant residual neurologic deficit
• Severe chronic obstructive pulmonary disease with Forced Expiratory Volume in 1 Second (FEV1) < 45% of predicted value
• Home oxygen use
• Previous difficult intubation
• Acute normovolemic blood conservation techniques
• Liver disease with serum aspartate aminotransferase (AST) > 31 U/L
• Circulatory arrest
• Thrombolysis
• Pre-existing clotting disorder
• Platelet receptor glycoprotein IIb/IIIa (GP IIb/IIIa) antagonist medication received within 48 hours
• Steroids
• Ejection Fraction < 40%
• Intra-aortic balloon pumps
• Ongoing congestive heart failure
• Ventricular assist devices
• Total hearts
• Pregnant women

Where it is running

• Mayo Clinic in Rochester — Rochester, Minnesota, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.