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The Efficacy and Safety of Hypertonic Saline in Cardiac Surgery Patients. (ESHHS)

Primary Purpose

Coronary Artery Disease, Edema

Status
Completed
Phase
Phase 2
Locations
Russian Federation
Study Type
Interventional
Intervention
7.2% NaCl plus 6% hydroxyethyl starch 200/0.5
0.9% NaCl
Sponsored by
Meshalkin Research Institute of Pathology of Circulation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Coronary Artery Disease focused on measuring Organ dysfunction, Hypertonic solution, Extravascular water, Cardiopulmonary Bypass

Eligibility Criteria

30 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients scheduled for first-time coronary artery bypass grafting with cardiopulmonary bypass

Exclusion Criteria:

  • age >70 years
  • body mass index <18 and >35 kg/m2
  • left ventricular ejection fraction <40%
  • myocardial infarction <6 months before surgery
  • stroke or transient ischemic attack <12 months before surgery
  • diabetes mellitus
  • glomerular filtration rate <90 mL/min
  • emergency surgery
  • hematocrit <30%.

Sites / Locations

  • Novosibirsk Research Institute of Pathology of Circulation

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

7.2% NaCl /hydroxyethyl starch 200/0.5

0.9% NaCl

Arm Description

On-pump CABG. 7.2% NaCl plus 6% hydroxyethyl starch 200/0.5 solution (HyperHAES) 4 mL/kg for 30 min, IV (in the vein), once, starting after the first hemodynamic measurement is obtained (before the beginning of CPB)

On-pump CABG. 0.9% NaCl (isotonic saline) 4 mL/kg for 30 min, IV (in the vein), once, starting after the first hemodynamic measurement is obtained (before the beginning of CPB)

Outcomes

Primary Outcome Measures

Extravascular Lung Water Index
Extravascular lung water index (ELWI; mL/kg) will be used to assess this outcome measure. ELWI was monitored by transcardiopulmonary thermodilution technique with the PiCCO plus system. Extravascular lung water represents the extravascular fluid of the lung tissue. It includes intra-cellular, interstitial and intra-alveolar water (not pleural effusion). It is indexed to "Predicted Body Weight".

Secondary Outcome Measures

Pulmonary Oxygenation
Index of arterial oxygenation efficiency (PaO2/FiO2), alveolar-arterial oxygen tension difference (AaDO2) will be used to assess this outcome measure.
Oxygen Delivery
Oxygen delivery index (DO2I) will be used to assess this outcome measure.
Cardiac Index
Fluid Balance
Net fluid balance at the end of surgery equals the sum of all infusions minus the urine output. Net fluid balance at postoperative day 1 equals the sum of all infusions minus the urine output and blood loss.
Inflammation Response
Serum levels of Interleukin 6 (IL-6) and Interleukin 10 (IL-10) will be used to assess this outcome measure.
Endothelial Integrity
Serum levels of intercellular adhesion molecule-1 (ICAM-1), E-selectin will be used to assess this outcome measure.
Plasma Na
Plasma Osmolarity
Rate of Acute Kidney Injury
serum creatinine, serum cystatin C, urine neutrophil gelatinase-associated lipocalin (uNGAL) will be used to asses this outcome measure.
Rate of Hyperchloremic Metabolic Acidosis
blood pH, base excess (BE), plasma level of Cl will be used to assess this outcome measure.
Stroke Volume Index
Rate of Neurological Complications
Delirium, clinically diagnosed stroke, and encephalopathy.
Blood Loss
Bleeding from chest tubes
Duration of Mechanical Ventilation
Chloride Loading
The amount of chloride ions (mmol per patient) which will be infused during the surgery and ICU stay

Full Information

First Posted
August 5, 2012
Last Updated
April 29, 2016
Sponsor
Meshalkin Research Institute of Pathology of Circulation
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1. Study Identification

Unique Protocol Identification Number
NCT01675453
Brief Title
The Efficacy and Safety of Hypertonic Saline in Cardiac Surgery Patients.
Acronym
ESHHS
Official Title
The Efficacy and Safety of 7.2% NaCl Plus 6% Hydroxyethyl 200/0.5 in Patients Scheduled for First-time Coronary Artery Bypass Grafting With Cardiopulmonary Bypass.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
September 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Meshalkin Research Institute of Pathology of Circulation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The organ dysfunction following cardiopulmonary bypass (CPB) occurs frequently in cardiac surgery patients. Systemic inflammatory response initiated by CPB through releasing of several mediators lead to altered endothelial integrity and in consequence the leakage of proteins and fluids from the intravascular to the interstitial compartment is occurred. Increased capillary permeability and decreased colloid osmotic pressure were shown to play a key role for fluid shift and increasing of extravascular water. Further tissue edema can result in injury to many organs, including the heart, lungs, brain, kidneys and can lead to adverse outcomes. Hypertonic solution creates an osmotic gradient across the cellular membrane, causing a fluid shift from the intracellular and the interstitial spaces of tissue into the intravascular compartment. The purpose of this study is to investigate the efficacy and safety of 7.2% NaCl plus 6% hydroxyethyl starch 200/0.5 in patients scheduled for first-time coronary artery bypass grafting with cardiopulmonary bypass.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Edema
Keywords
Organ dysfunction, Hypertonic solution, Extravascular water, Cardiopulmonary Bypass

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
7.2% NaCl /hydroxyethyl starch 200/0.5
Arm Type
Active Comparator
Arm Description
On-pump CABG. 7.2% NaCl plus 6% hydroxyethyl starch 200/0.5 solution (HyperHAES) 4 mL/kg for 30 min, IV (in the vein), once, starting after the first hemodynamic measurement is obtained (before the beginning of CPB)
Arm Title
0.9% NaCl
Arm Type
Placebo Comparator
Arm Description
On-pump CABG. 0.9% NaCl (isotonic saline) 4 mL/kg for 30 min, IV (in the vein), once, starting after the first hemodynamic measurement is obtained (before the beginning of CPB)
Intervention Type
Drug
Intervention Name(s)
7.2% NaCl plus 6% hydroxyethyl starch 200/0.5
Other Intervention Name(s)
HyperHAES
Intervention Type
Drug
Intervention Name(s)
0.9% NaCl
Other Intervention Name(s)
Saline
Primary Outcome Measure Information:
Title
Extravascular Lung Water Index
Description
Extravascular lung water index (ELWI; mL/kg) will be used to assess this outcome measure. ELWI was monitored by transcardiopulmonary thermodilution technique with the PiCCO plus system. Extravascular lung water represents the extravascular fluid of the lung tissue. It includes intra-cellular, interstitial and intra-alveolar water (not pleural effusion). It is indexed to "Predicted Body Weight".
Time Frame
baseline; 5 min after infusion; 5 min after CPB; 30 min after CPB; end of surgery; 2 h, 4 h, 6 h, 12 h after CPB; Postoperative day 1
Secondary Outcome Measure Information:
Title
Pulmonary Oxygenation
Description
Index of arterial oxygenation efficiency (PaO2/FiO2), alveolar-arterial oxygen tension difference (AaDO2) will be used to assess this outcome measure.
Time Frame
24 hours
Title
Oxygen Delivery
Description
Oxygen delivery index (DO2I) will be used to assess this outcome measure.
Time Frame
24 hours
Title
Cardiac Index
Time Frame
24 hours
Title
Fluid Balance
Description
Net fluid balance at the end of surgery equals the sum of all infusions minus the urine output. Net fluid balance at postoperative day 1 equals the sum of all infusions minus the urine output and blood loss.
Time Frame
24 hours
Title
Inflammation Response
Description
Serum levels of Interleukin 6 (IL-6) and Interleukin 10 (IL-10) will be used to assess this outcome measure.
Time Frame
24 hours
Title
Endothelial Integrity
Description
Serum levels of intercellular adhesion molecule-1 (ICAM-1), E-selectin will be used to assess this outcome measure.
Time Frame
24 hours
Title
Plasma Na
Time Frame
24 hours
Title
Plasma Osmolarity
Time Frame
24 hours
Title
Rate of Acute Kidney Injury
Description
serum creatinine, serum cystatin C, urine neutrophil gelatinase-associated lipocalin (uNGAL) will be used to asses this outcome measure.
Time Frame
48 hours
Title
Rate of Hyperchloremic Metabolic Acidosis
Description
blood pH, base excess (BE), plasma level of Cl will be used to assess this outcome measure.
Time Frame
24 hours
Title
Stroke Volume Index
Time Frame
24 hours
Title
Rate of Neurological Complications
Description
Delirium, clinically diagnosed stroke, and encephalopathy.
Time Frame
24 hours
Title
Blood Loss
Description
Bleeding from chest tubes
Time Frame
24 hours
Title
Duration of Mechanical Ventilation
Time Frame
24 hours
Title
Chloride Loading
Description
The amount of chloride ions (mmol per patient) which will be infused during the surgery and ICU stay
Time Frame
24 h

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients scheduled for first-time coronary artery bypass grafting with cardiopulmonary bypass Exclusion Criteria: age >70 years body mass index <18 and >35 kg/m2 left ventricular ejection fraction <40% myocardial infarction <6 months before surgery stroke or transient ischemic attack <12 months before surgery diabetes mellitus glomerular filtration rate <90 mL/min emergency surgery hematocrit <30%.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vladimir V Lomivorotov, MD, PhD
Organizational Affiliation
Novosibirsk Research Institute of Pathology of Circulation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Novosibirsk Research Institute of Pathology of Circulation
City
Novosibirsk
State/Province
Novosibirsk territory
ZIP/Postal Code
630055
Country
Russian Federation

12. IPD Sharing Statement

Citations:
PubMed Identifier
24549094
Citation
Lomivorotov VV, Fominskiy EV, Efremov SM, Nepomniashchikh VA, Lomivorotov VN, Chernyavskiy AM, Shilova AN, Karaskov AM. Infusion of 7.2% NaCl/6% hydroxyethyl starch 200/0.5 in on-pump coronary artery bypass surgery patients: a randomized, single-blind pilot study. Shock. 2014 Mar;41(3):193-9. doi: 10.1097/SHK.0000000000000087.
Results Reference
derived

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The Efficacy and Safety of Hypertonic Saline in Cardiac Surgery Patients.

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