Preventing Contrast Nephropathy With Sodium Bicarbonate in Patients With Pulmonary Edema,Heart Failure,Uncontrolled HTN
Primary Purpose
Contrast Induced Nephropathy
Status
Completed
Phase
Phase 2
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Sodium Bicarbonate
Sponsored by
About this trial
This is an interventional prevention trial for Contrast Induced Nephropathy focused on measuring Contrast Nephropathy, Sodium Bicarbonate, Prevention
Eligibility Criteria
Inclusion Criteria:
- individuals aged 18 years or older with serum creatinine levels of at least 1.5 mg/dl , who were scheduled to undergo diagnostic or therapeutic coronary artery angiography.
- Patients with a history of Pulmonary edema or
- Patients with severe Heart Failure ( NYHA 3-4) or
- Patients with ejection fraction of less than 30% on Echocardiography ( done in the previous month of admission) or
- Patients with uncontrolled hypertension (treated systolic blood pressure more than 160 mmHg, or diastolic blood pressure more than 100mmHg )
Exclusion Criteria:
- serum creatinine levels of more than 8 mg/dl
- previous history of dialysis
- GFR < 20 ( as calculated with this formula: ((140-Age)(Weight(Kg)) / Serum Creatinine(mg/dl) ×72 ) , in females GFR was multiplied by 0.85 )
- emergency catheterization
- recent exposure to radiographic contrast agents (within previous two days of the study)
- radiocontrast agent dosage needed more than 300 gr during the procedure
- allergy to radiocontrast agent
- pregnancy
- administration of dopamine, mannitol , fenoldopam or N-Acetyl Cystein during the intended time of study
- need for continuous hydration therapy (e.g. sepsis )
- history of Multiple myeloma
Sites / Locations
- Tehran Heart Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
1
2
Arm Description
1075 cc of 77 mEq/L solution of NaCl 0.45% , prepared by adding 75 cc of 77 mEq/L NaCl 0.45 % to 1000 cc of 77 mEq/L NaCl 0.45%
1075 cc fluid made by adding 75 cc of sodium bicarbonate solution 8.4% to 1000 cc of NaCl 0.45%.
Outcomes
Primary Outcome Measures
development of contrast induced nephropathy defined as an absolute (> or = 0.5 mg/dl) or relative increase (> or = 25%) in serum creatinine at 48 hours after exposure to a contrast agent compared to baseline serum creatinine values.
Secondary Outcome Measures
an absolute (> or = 0.5 mg/dl) or relative increase(> or= 25% ) in serum creatinine at day 5 after exposure to a contrast agent.
Urine PH after initial bolus
development of contrast induced nephropathy defined as 25% decrease in glomerular filtration rate (GFR) at 48 hours.
development of contrast induced nephropathy defined as 25% decrease in glomerular filtration rate (GFR)on day 5 .
Full Information
NCT ID
NCT00513825
First Posted
August 8, 2007
Last Updated
November 23, 2008
Sponsor
Tehran University of Medical Sciences
Collaborators
Tehran Heart Center
1. Study Identification
Unique Protocol Identification Number
NCT00513825
Brief Title
Preventing Contrast Nephropathy With Sodium Bicarbonate in Patients With Pulmonary Edema,Heart Failure,Uncontrolled HTN
Official Title
The Evaluation of the Effect of Sodium Bicarbonate Solution in Decreasing the Incidence of Contrast Induced Nephropathy (CIN) in Patients With Pulmonary Edema,Severe Heart Failure or Uncontrolled Hypertension
Study Type
Interventional
2. Study Status
Record Verification Date
November 2008
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
July 2008 (Actual)
Study Completion Date
July 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Tehran University of Medical Sciences
Collaborators
Tehran Heart Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Radio Contrast Induced Nephropathy (RCIN) remains a well recognized complication in patients undergoing diagnostic or interventional procedures requiring radiographic contrast agents. Recent studies have shown benefit in administering Sodium Bicarbonate over normal saline( the uniformly accepted prophylaxy) in preventing RCIN.But most studies have excluded patients with history of pulmonary edema, severe heart failure(NYHA 3-4), uncontrolled hypertension or ejection fraction less than 30%. Therefore the aim of this study is to evaluate the efficacy of sodium bicarbonate solved in half saline compared with infusion of half saline in prevention of RCIN in these groups of patients.
Detailed Description
Radio Contrast Induced Nephropathy (RCIN) remains a well recognized complication in patients undergoing diagnostic or interventional procedures requiring radiographic contrast agents and is the third leading cause of acquired acute renal failure in hospitalized patients. Strategies for the prevention of radiocontrast nephropathy have focused on countering vasoconstriction (pre-hydration, fenoldopam, and theophylline), enhancing flow through the nephron (diuretics), or protection against oxygen-free-radical injury (urinary alkalinization and N-acetylcysteine).
Among all prophylactic measures that have been proposed, adequate preprocedural and postprocedural hydration has demonstrated effectiveness in the prevention of radiocontrast nephropathy. Thus, it remains the most frequently applied measure in clinical practice.
A Recent study in May 2004 have shown benefit in administering Sodium Bicarbonate over normal saline as a prophylaxy.Since alkalizing renal tubular fluid with bicarbonate may reduce injury .
Most studies have excluded patients with history of pulmonary edema, severe heart failure(NYHA 3-4), uncontrolled hypertension or ejection fraction less than 30% and no specific protocol is tested for this group of patients. This study focuses on preventing RCIN in this specific group of patients .
Comparisons:1075 cc NaCl 0.45% or 75 cc of sodium bicarbonate 8.4% solved in one liter of NaCl 0.45%. Each fluid is infused at the rate of 3 ml/kg/ hour one hour before the angiographic procedure, continuing at the rate of 1 ml/kg/ hour for 6 hours after the procedure. Maximum rate of fluid permitted is that for a body weight of 110 Kg.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Contrast Induced Nephropathy
Keywords
Contrast Nephropathy, Sodium Bicarbonate, Prevention
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
72 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
1075 cc of 77 mEq/L solution of NaCl 0.45% , prepared by adding 75 cc of 77 mEq/L NaCl 0.45 % to 1000 cc of 77 mEq/L NaCl 0.45%
Arm Title
2
Arm Type
Active Comparator
Arm Description
1075 cc fluid made by adding 75 cc of sodium bicarbonate solution 8.4% to 1000 cc of NaCl 0.45%.
Intervention Type
Drug
Intervention Name(s)
Sodium Bicarbonate
Intervention Description
IV solution of NaCl 0.45% (Arm 1) or IV 75 cc of sodium bicarbonate 8.4% solved in 1 liter of NaCl 0.45% (Arm 2) . Each fluid is infused at the rate of 3 ml/kg/ hour one hour before the angiographic procedure, continuing at the rate of 1 ml/kg/ hour for 6 hours after the procedure. Maximum rate of fluid permitted is that for a body weight of 110 Kg.
Primary Outcome Measure Information:
Title
development of contrast induced nephropathy defined as an absolute (> or = 0.5 mg/dl) or relative increase (> or = 25%) in serum creatinine at 48 hours after exposure to a contrast agent compared to baseline serum creatinine values.
Time Frame
at 48 hours
Secondary Outcome Measure Information:
Title
an absolute (> or = 0.5 mg/dl) or relative increase(> or= 25% ) in serum creatinine at day 5 after exposure to a contrast agent.
Time Frame
at day 5
Title
Urine PH after initial bolus
Time Frame
within 6 hours after initial bolus
Title
development of contrast induced nephropathy defined as 25% decrease in glomerular filtration rate (GFR) at 48 hours.
Time Frame
at 48 hours
Title
development of contrast induced nephropathy defined as 25% decrease in glomerular filtration rate (GFR)on day 5 .
Time Frame
on day 5 post contrast
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
individuals aged 18 years or older with serum creatinine levels of at least 1.5 mg/dl , who were scheduled to undergo diagnostic or therapeutic coronary artery angiography.
Patients with a history of Pulmonary edema or
Patients with severe Heart Failure ( NYHA 3-4) or
Patients with ejection fraction of less than 30% on Echocardiography ( done in the previous month of admission) or
Patients with uncontrolled hypertension (treated systolic blood pressure more than 160 mmHg, or diastolic blood pressure more than 100mmHg )
Exclusion Criteria:
serum creatinine levels of more than 8 mg/dl
previous history of dialysis
GFR < 20 ( as calculated with this formula: ((140-Age)(Weight(Kg)) / Serum Creatinine(mg/dl) ×72 ) , in females GFR was multiplied by 0.85 )
emergency catheterization
recent exposure to radiographic contrast agents (within previous two days of the study)
radiocontrast agent dosage needed more than 300 gr during the procedure
allergy to radiocontrast agent
pregnancy
administration of dopamine, mannitol , fenoldopam or N-Acetyl Cystein during the intended time of study
need for continuous hydration therapy (e.g. sepsis )
history of Multiple myeloma
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ali Farahani Vasheghani, M.D.
Organizational Affiliation
Tehran University of Medical Sciences, Tehran Heart Center
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ebrahim Kassaian, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Akbar Fotuhi, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mohammad Reza Khatami, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mojtaba Salarifar, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ebrahim Nematipur, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ahmad Iaminisharif, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Saeid Sadeghian, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ali mohammad Hajzeinali, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mohammad Alidoosti, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hamidreza Purhosseini,, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ali Kazemisaeid, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gholamreza Davoodi, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Alireza Amirzadegan, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Abbas Soleimani, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sirus Darabian, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kianush Hossein, M.D.
Organizational Affiliation
Tehran Heart Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gelareh Sadigh, M.D.
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Amir Hossein Razavi, M.D.
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tehran Heart Center
City
Tehran
Country
Iran, Islamic Republic of
12. IPD Sharing Statement
Learn more about this trial
Preventing Contrast Nephropathy With Sodium Bicarbonate in Patients With Pulmonary Edema,Heart Failure,Uncontrolled HTN
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