Trial record 6 of 7 for:
"Exsanguination"
Impact of Fluid Restriction Policy in Reducing the Use of Red Cells in Cardiac Surgery
This study has been completed.
Sponsor:
Larissa University Hospital
Information provided by:
Larissa University Hospital
ClinicalTrials.gov Identifier:
NCT00600704
First received: January 14, 2008
Last updated: May 9, 2011
Last verified: March 2011
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Purpose
The investigators' hypothesis is that restriction of circulating fluids in comparison to a liberal fluid administration policy would lead to a reduction of allogenic red blood cells exposure in patients undergoing cardiopulmonary bypass (CPB) for primary coronary artery bypass graft supported by reinfusion of washed shed blood from thoracic cavities.
| Condition | Intervention |
|---|---|
| Coronary Artery Disease Coronary Artery Bypass Erythrocyte Transfusion | Procedure: Fluid Restriction Policy Procedure: Free fluid infusion |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Care Provider, Investigator) Primary Purpose: Supportive Care |
| Official Title: | Impact of Fluid Restriction Policy Added to Intra-Operative Cell Salvage in Reducing the Use of Red Cells in Cardiac Surgery |
Further study details as provided by Larissa University Hospital:
Primary Outcome Measures:
- Mean Number of Packed Red Cells Units Transfused During Hospital Stay [ Time Frame: 20 months ]
| Enrollment: | 192 |
| Study Start Date: | November 2007 |
| Study Completion Date: | March 2011 |
| Primary Completion Date: | November 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: RESTRICTED FLUIDS
Infusion of Hes 130/0.4 up to 500 ml until the beginning of Cardiopulmonary Bypass
|
Procedure: Fluid Restriction Policy
Infusion of Hes 130/0.4 up to 500 ml until the beginning of Cardiopulmonary bypass
|
|
Active Comparator: FREE FLUIDS
Free fluid infusion unless Hb< 6g/dl(allogenic blood use), until the beginning of Cardiopulmonary bypass
|
Procedure: Free fluid infusion
Free fluid infusion unless Hb< 6g/dl(allogenic blood use), until the beginning of Cardiopulmonary bypass
|
Detailed Description:
192 patients operated under equal conditions were assigned prospectively and randomly either for a restrictive protocol for intravenous fluid administration (group A, 100 patients) or not (group B, 92 patients). Transfusion guidelines were common for the two groups. The volumes of intravenous fluids, priming, "extra" volume on pump and cardioplegic solution and the volume of urine were recorded. Net erythrocyte volume loss was calculated. The number of the transfused PRC was analyzed as a continuous variable. "Transfusion" was analyzed as a categorical characteristic. Analysis employed Student's two-tailed t-test, t-paired test and chitest.
Eligibility| Ages Eligible for Study: | Child, Adult, Senior |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Ejection fraction (EF) of left ventricle (LV) > 35%
- Preoperative serum Creatinine < 150 μmol/l
- Preoperative Haemoglobin > 10/dl
- Peripheral anastomosis scheduled =< 3
Exclusion Criteria:
- redo bypass-emergency operations
- prior coronal stenting
- active congestive heart failure
- documented Myocardial Infraction within the previous 6 weeks
- NYHA class > 3
- Carotid stenosis > 50%
- CVA
- INR > 1.5
- chronic obstructive pulmonary disease (COPD)
- Steroid therapy-chronic inflammatory process
- Use of aprotinin or tranexamic acid
Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00600704
Please refer to this study by its ClinicalTrials.gov identifier: NCT00600704
Locations
| Greece | |
| Larissa University Hospital | |
| Larissa, Thesalia, Greece, 41110 | |
Sponsors and Collaborators
Larissa University Hospital
Investigators
| Principal Investigator: | ATHINA KLEITSAKI, Dr | Larissa University Hospital |
| Study Director: | GEORGE VRETZAKIS, M.D. PhD | Cardiac Anesthesia Unit, Department of Anesthesiology, University Hospital of Larissa, Greece |
| Study Chair: | KONSTANTINOS STAMOULIS, M.D. | Cardiac Anesthesia Unit, Department of Anesthesiology, University Hospital of Larissa, Greece |
| Study Chair: | CHRISTOS DRAGOUMANIS, M.D. PhD | Cardiac Anesthesia Unit, Department of Anesthesiology, University Hospital of Larissa, Greece |
| Study Chair: | VASILIOS TASOUDIS, M.D. | Cardiac Anesthesia Unit, Department of Anesthesiology, University Hospital of Larissa, Greece |
| Study Chair: | KATERINA KYRIAKAKI, M.D. | Cardiac Anesthesia Unit, Department of Anesthesiology, University Hospital of Larissa, Greece |
| Study Chair: | DEMETRIOS MIKROULIS, M.D. PhD | Department of Cardiothoracic Surgery, University Hospital of Larissa, Greece |
| Study Chair: | ATHANASIOS GIANNOUKAS, MD MSc PhD | Department of Vascular Surgery, University Hospital of Larissa, Greece |
| Study Chair: | NIKOLAOS TSILIMINGAS, M.D. PhD | Department of Cardiothoracic Surgery, University Hospital of Larissa, Greece |
More Information
Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | ATHINA KLEITSAKI, LARISSA UNIVERSITY HOSPITAL/DPT OF ANESTHESIOLOGY |
| ClinicalTrials.gov Identifier: | NCT00600704 History of Changes |
| Other Study ID Numbers: |
LUH 1975 AK POL 1969 TT |
| Study First Received: | January 14, 2008 |
| Results First Received: | March 4, 2011 |
| Last Updated: | May 9, 2011 |
Keywords provided by Larissa University Hospital:
|
Allogenic Blood Use Total Blood Loss Reinfusion of Washed Shed Blood |
Additional relevant MeSH terms:
|
Coronary Artery Disease Myocardial Ischemia Coronary Disease Heart Diseases |
Cardiovascular Diseases Arteriosclerosis Arterial Occlusive Diseases Vascular Diseases |
ClinicalTrials.gov processed this record on July 13, 2017


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