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Albumin Versus Hydroxyethyl Starch in Cardiopulmonary Bypass Surgery

Comparing the effects of 5% albumin and 6% hydroxyethyl starch 130/0.4 on glomerular filtration rate and serum creatinine when used as priming solutions for cardiopulmonary bypass pump.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015011620112N4
Enrollment
60
Registered
2015-02-04
Start date
2012-01-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Atherosclerotic heart disease. Atherosclerotic heart disease

Interventions

Intervention 1: 500 milliliter human albumin 5% as a priming solution of cardiopulmonary bypass pump. Intervention 2: 500 milliliter 6% hydroxyethyl starch 130/0.4 as priming solution of cardiopulmona
Treatment - Drugs
500 milliliter human albumin 5% as a priming solution of cardiopulmonary bypass pump.
500 milliliter 6% hydroxyethyl starch 130/0.4 as priming solution of cardiopulmonary bypass pump

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients undergoing elective coronary artery bypass grafting; age between 30 - 60 . Exclusion criteria: chronic renal failure; cardiopulmonary by pass pomp time over 2 hours; Patients were underwent an emergency operation; infective endocarditis; preoperative coagulation disorder; liver insufficiency; a left ventricular ejection fraction of less than 50%; previous cardiac surgery; a hemoglobin level of less than 10 milligram per deciliter before surgery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Serum Creatinine. Timepoint: preoprative and every 24 houre to 72 hour postoperatively. Method of measurement: isotope dilution mass spectrometry.

Secondary

MeasureTime frame
Glomerular filtration rate. Timepoint: preoperative and Every 24 hour to 72 hour postoperatively. Method of measurement: isotope dilution mass spectrometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPooya Derakhshan

Birjand University of Medical Sciences

pooyaderkh@yahoo.com00

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026