Simvastatin For Intracerebral Hemorrhage Study
Primary Purpose
Intracerebral Hemorrhage
Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Simvastatin 80 mg
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Intracerebral Hemorrhage focused on measuring Intracerebral, Hemorrhage, Edema, Statins
Eligibility Criteria
Inclusion Criteria:
- Patient with CT evidence of ICH admitted within 24 hours of onset of symptoms.
Exclusion Criteria:
- Age < 18 or > 85
- Admission Glasgow Coma Score (GCS) < 6
- ICH volume < 10 cc
- ICH secondary to trauma, aneurysm, Arterio-Venous Malformation (AVM), tumor or post surgical
- Multiple ICH
- Associated Subdural hematoma or significant Subarachnoid hemorrhage
- History of prior neurologic disease with modified Rankin Scale (mRS) > 1
- Hematoma evacuation, hemicraniectomy, clot lysis
- Myopathy
- Active Liver disease
- Pregnancy
- Statin allergy
- Patients on statins prior to admission
- Patients with an acute indication for statin therapy (Unstable angina)
Sites / Locations
- Johns Hopkins Bayview Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
I
II
Arm Description
Simvastatin Group
Placebo Group
Outcomes
Primary Outcome Measures
Perihematomal Edema
Solitary patient lost to follow up (out of state)
Secondary Outcome Measures
Full Information
NCT ID
NCT00718328
First Posted
July 15, 2008
Last Updated
September 8, 2017
Sponsor
Johns Hopkins University
Collaborators
National Center for Research Resources (NCRR), National Institutes of Health (NIH)
1. Study Identification
Unique Protocol Identification Number
NCT00718328
Brief Title
Simvastatin For Intracerebral Hemorrhage Study
Official Title
Simvastatin For Intracerebral Hemorrhage Study
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Terminated
Why Stopped
Poor recruitment, trial terminated
Study Start Date
October 2008 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
June 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
National Center for Research Resources (NCRR), National Institutes of Health (NIH)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Study Objective: To analyze if statins are effective in ameliorating perihematomal edema evolution thereby reducing mortality and improving functional outcomes following spontaneous intracerebral hemorrhage (ICH).
Detailed Description
Intracerebral hemorrhage (ICH) causes 10% to 15% of first-ever strokes, with a 30-day mortality rate of 35% to 52% with only 20% expected to be functionally independent at 6 months. No medical or surgical interventions have been found to alter the natural evolution of this disease. The high risk for mortality and poor outcomes seems to occur despite relatively small hematoma volumes and small amounts of neuronal tissue at risk for injury. The reasons for this observation remain unknown; however perihematomal edema formation and inflammation that follows ICH seems to play an important role.
The Simvastatin for Intracerebral Hemorrhage Study is a prospective double blinded placebo controlled randomized (1:1) clinical trial that compares outcomes in patients receiving generic simvastatin 80 mg for 14 days or until death or discharge with patients in the placebo group.
The hypothesis for our study is that statins ameliorate perihematomal edema evolution thereby reducing mortality and improving functional outcomes following Intracerebral Hemorrhage (ICH). This hypothesis in turn is based on animal data showing suppression of inflammatory reaction and improved neurological outcomes following administration of statins to rodents with experimental ICH, and on a retrospective review of patients admitted to The Johns Hopkins Hospital over the last 7 years with spontaneous ICH which showed significantly better outcomes (decreased 30 day mortality secondary to decreased perihematomal edema) in patients on statins at the time of admission.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intracerebral Hemorrhage
Keywords
Intracerebral, Hemorrhage, Edema, Statins
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1 (Actual)
8. Arms, Groups, and Interventions
Arm Title
I
Arm Type
Experimental
Arm Description
Simvastatin Group
Arm Title
II
Arm Type
Placebo Comparator
Arm Description
Placebo Group
Intervention Type
Drug
Intervention Name(s)
Simvastatin 80 mg
Intervention Description
Patients in study arm 1 will receive simvastatin 80 mg once daily for 14 days or until death or discharge.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Patients in study arm II will receive placebo once daily for 14 days or until death or discharge.
Primary Outcome Measure Information:
Title
Perihematomal Edema
Description
Solitary patient lost to follow up (out of state)
Time Frame
Days 7 and 14
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient with CT evidence of ICH admitted within 24 hours of onset of symptoms.
Exclusion Criteria:
Age < 18 or > 85
Admission Glasgow Coma Score (GCS) < 6
ICH volume < 10 cc
ICH secondary to trauma, aneurysm, Arterio-Venous Malformation (AVM), tumor or post surgical
Multiple ICH
Associated Subdural hematoma or significant Subarachnoid hemorrhage
History of prior neurologic disease with modified Rankin Scale (mRS) > 1
Hematoma evacuation, hemicraniectomy, clot lysis
Myopathy
Active Liver disease
Pregnancy
Statin allergy
Patients on statins prior to admission
Patients with an acute indication for statin therapy (Unstable angina)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Neeraj S Naval, M.D.
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins Bayview Medical Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
17701108
Citation
Naval NS, Abdelhak TA, Zeballos P, Urrunaga N, Mirski MA, Carhuapoma JR. Prior statin use reduces mortality in intracerebral hemorrhage. Neurocrit Care. 2008;8(1):6-12. doi: 10.1007/s12028-007-0080-2.
Results Reference
background
PubMed Identifier
17701107
Citation
Naval NS, Abdelhak TA, Urrunaga N, Zeballos P, Mirski MA, Carhuapoma JR. An association of prior statin use with decreased perihematomal edema. Neurocrit Care. 2008;8(1):13-8. doi: 10.1007/s12028-007-0081-1.
Results Reference
background
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Simvastatin For Intracerebral Hemorrhage Study
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