Clinical and Economic Outcome of Simvastatin in Critically Ill Septic Patient
Primary Purpose
Critical Illness
Status
Completed
Phase
Phase 3
Locations
Egypt
Study Type
Interventional
Intervention
Simvastatin
Sponsored by
About this trial
This is an interventional treatment trial for Critical Illness
Eligibility Criteria
Inclusion criteria:-
- Age >18 and less than 70
- Sepsis for less than 24 hours from ICU admission
Exclusion criteria:-
- Elderly (defined as older than 70).
- Pediatrics (defined as younger than 18).
- Pregnancy and nursing.
- Unable to receive enteral medications.
- History of hypersensitivity to the trial drug.
- Are receiving drugs known to interact with simvastatin.
- Acute liver failure and chronic liver disease (Child C).
- High risk of rhabdomyolysis (multiple traumas, crush injuries, extensive burns(>60%), baseline creatinine kinase (CK) ≥ten-times upper limit of normal.
- Patients with dyslipidemia or Prior statin user.
- Sever renal impairment (defined as need for replacement therapy )and uncontrolled hypothyroidism
- Have a history of known or suspected porphyria
- Are unlikely to survive more than 24 hours
Sites / Locations
- Ain shams university hospital and cairo university hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Active Comparator
Arm Label
broad spectrum AB +fluids
simvastatin
Arm Description
Control group :50 patients will be treated according to SURVIVING SEPSIS CAMPAIGN BUNDLES
50 patients will be treated according SSCG plus simvastatin as single oral tablet 40 mg / day begin with inclusion in the study and continue until hospital discharge .If the patient is able to swallow; the tablet will be given orally. Otherwise, it will be crushed, suspended in water and administered via any existing enteral feeding or gastric drainage tube. (White R, Bradnam V, 2013)
Outcomes
Primary Outcome Measures
28 day ICU and hospital mortality
Secondary Outcome Measures
Number of patients alive 3, 6, and 12 months and incremental cost effectiveness ratio
Full Information
NCT ID
NCT02067949
First Posted
February 19, 2014
Last Updated
April 3, 2015
Sponsor
sara mostafa amin eladawy
1. Study Identification
Unique Protocol Identification Number
NCT02067949
Brief Title
Clinical and Economic Outcome of Simvastatin in Critically Ill Septic Patient
Official Title
The Clinical Outcome and the Cost-effectiveness Analysis of Simvastatin Plus Standard Therapy Versus Standard Therapy Alone in Critically Ill Septic Patient"
Study Type
Interventional
2. Study Status
Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
February 2015 (Actual)
Study Completion Date
March 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
sara mostafa amin eladawy
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
determination of the effectiveness and the cost-effectiveness of simvastatin(Zocor 40 mg) plus standard therapy (SSCG)versus standard therapy alone in critically ill septic patient from the societal perspective over one year.
Detailed Description
Prospective double blinded randomized controlled study Will be carried out at Ain-Shams university hospital Method: - After approval of the research ethics committee of Ain shams University and obtaining consent from each patient, 100 patients newly admitted to the intensive care unit (ICU) diagnosed to have sepsis/severe sepsis defined by American College of Chest Physicians (ACP) *will be randomized by the clinical pharmacist using a computer-generated randomization sequence with a block size of four into two groups.
Group I (Control group):-50 patients will be treated according to "Surviving Sepsis Campaign guidelines (SSCG) (Dellinger, et al. 2013) Group II (Intervention group):-50 patients will be treated according SSCG plus simvastatin.
Outcomes:- Primary outcome measures: 28 day ICU and hospital mortality.
Secondary Outcome Measures:
Requirement and length of renal replacement therapy, vasoactive agent support or mechanical ventilation
Total ICU length of stay.(LOS)
Number of patients alive 3, 6, and 12 months
Incremental cost effectiveness ratio
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Illness
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
broad spectrum AB +fluids
Arm Type
No Intervention
Arm Description
Control group :50 patients will be treated according to SURVIVING SEPSIS CAMPAIGN BUNDLES
Arm Title
simvastatin
Arm Type
Active Comparator
Arm Description
50 patients will be treated according SSCG plus simvastatin as single oral tablet 40 mg / day begin with inclusion in the study and continue until hospital discharge .If the patient is able to swallow; the tablet will be given orally. Otherwise, it will be crushed, suspended in water and administered via any existing enteral feeding or gastric drainage tube. (White R, Bradnam V, 2013)
Intervention Type
Drug
Intervention Name(s)
Simvastatin
Other Intervention Name(s)
Zocor 40 mg
Intervention Description
single oral tablet 40 mg / day If the patient is able to swallow; the tablet will be given orally. Otherwise, it will be crushed, suspended in water and administered via any existing enteral feeding or gastric drainage tube
Primary Outcome Measure Information:
Title
28 day ICU and hospital mortality
Time Frame
one year
Secondary Outcome Measure Information:
Title
Number of patients alive 3, 6, and 12 months and incremental cost effectiveness ratio
Time Frame
one year
Other Pre-specified Outcome Measures:
Title
ICU hazards
Description
Requirement and length of renal replacement therapy, vasoactive agent support or mechanical ventilation
Total ICU length of stay.(LOS)
Time Frame
one year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:-
Age >18 and less than 70
Sepsis for less than 24 hours from ICU admission
Exclusion criteria:-
Elderly (defined as older than 70).
Pediatrics (defined as younger than 18).
Pregnancy and nursing.
Unable to receive enteral medications.
History of hypersensitivity to the trial drug.
Are receiving drugs known to interact with simvastatin.
Acute liver failure and chronic liver disease (Child C).
High risk of rhabdomyolysis (multiple traumas, crush injuries, extensive burns(>60%), baseline creatinine kinase (CK) ≥ten-times upper limit of normal.
Patients with dyslipidemia or Prior statin user.
Sever renal impairment (defined as need for replacement therapy )and uncontrolled hypothyroidism
Have a history of known or suspected porphyria
Are unlikely to survive more than 24 hours
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
sara M amin, MSC
Organizational Affiliation
Ain Shams University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ain shams university hospital and cairo university hospital
City
Cairo
ZIP/Postal Code
11361
Country
Egypt
12. IPD Sharing Statement
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Clinical and Economic Outcome of Simvastatin in Critically Ill Septic Patient
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