Sildenafil for DCI
Primary Purpose
Subarachnoid Hemorrhage, Cerebral Vasospasm
Status
Unknown status
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Low dose sildenafil citrate
High dose sildenafil citrate
Sponsored by
About this trial
This is an interventional treatment trial for Subarachnoid Hemorrhage
Eligibility Criteria
Inclusion Criteria:
- Age >= 21
- Onset of symptoms within 72 hours from presentation
- Subarachnoid hemorrhage from ruptured cerebral aneurysm
- Cerebral vasospasm diagnosed on transcranial doppler, CT angiography, or digital subtraction angiography
Exclusion Criteria:
- Pregnancy
- Subarachnoid hemorrhage secondary to traumatic or mycotic aneurysm
- Pre-ictal sildenafil therapy (last dose within 1 week of presentation)
- Contraindications to sildenafil therapy (i.e. use of nitrates, left ventricular outflow obstruction, impaired autonomic blood pressure control)
Sites / Locations
- University of Mississippi Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Low dose sildenafil
High dose sildenafil
Arm Description
Twelve patients with cerebral vasospasm following aneurysmal subarachnoid hemorrhage will be assigned to low dose sildenafil citrate and will receive a 20mg oral dose and a subsequent 10mg intravenous dose of sildenafil citrate.
Twelve patients with cerebral vasospasm following aneurysmal subarachnoid hemorrhage will be assigned to high dose sildenafil citrate and will receive a 60mg oral dose and a subsequent 30mg intravenous dose of sildenafil citrate.
Outcomes
Primary Outcome Measures
Change from baseline in mean arterial blood pressure
Area under the plasma concentration versus time curve (AUC) of sildenafil
Secondary Outcome Measures
Area under the cerebral spinal fluid concentration versus time curve (AUC) of sildenafil
Change from baseline in cerebral autoregulation
Full Information
NCT ID
NCT03028298
First Posted
January 13, 2017
Last Updated
June 5, 2021
Sponsor
University of Mississippi Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT03028298
Brief Title
Sildenafil for DCI
Official Title
Sildenafil for the Treatment of Delayed Cerebral Ischemia Following Subarachnoid Hemorrhage
Study Type
Interventional
2. Study Status
Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 2016 (undefined)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
July 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Mississippi Medical Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Each year, approximately 30,000 people in the United States suffer an intra-cranial hemorrhage due to aneurysmal rupture. Of those surviving the initial event, up to 40% will go on to have further neurological injury secondary to stroke (delayed cerebral ischemia) caused by constriction of blood vessels (i.e. vasospasm). Previous studies have shown that the medication sildenafil, given intravenously, improves vasospasm, but has an associated degree of hypotension. The degree of hypotension was well within safety thresholds for these patients.
Sildenafil is a medication that strongly inhibits the protein phosphodiesterase-V (PDE-V). The hypothesis for this study is that oral sildenafil will also improve vasospasm, but does not result in as much hypotension. Specifically, the investigators look to show that comparable doses of oral sildenafil produces the same degree of PDE-V inhibition as an intravenous dose while the degree of hypotension is reduced. Additionally, using measurements of cerebral blood flow regulation acquired using transcranial Doppler ultrasound, the investigators look to show that oral sildenafil produces the same degree of improvement in vasospasm and blood flow regulation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Subarachnoid Hemorrhage, Cerebral Vasospasm
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Patients will be randomly assigned to either low dose sildenafil (20mg oral and 10mg intravenous) or high dose sildenafil (60mg oral and 30 mg intravenous)
Masking
None (Open Label)
Allocation
Randomized
Enrollment
24 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Low dose sildenafil
Arm Type
Experimental
Arm Description
Twelve patients with cerebral vasospasm following aneurysmal subarachnoid hemorrhage will be assigned to low dose sildenafil citrate and will receive a 20mg oral dose and a subsequent 10mg intravenous dose of sildenafil citrate.
Arm Title
High dose sildenafil
Arm Type
Experimental
Arm Description
Twelve patients with cerebral vasospasm following aneurysmal subarachnoid hemorrhage will be assigned to high dose sildenafil citrate and will receive a 60mg oral dose and a subsequent 30mg intravenous dose of sildenafil citrate.
Intervention Type
Drug
Intervention Name(s)
Low dose sildenafil citrate
Intervention Type
Drug
Intervention Name(s)
High dose sildenafil citrate
Primary Outcome Measure Information:
Title
Change from baseline in mean arterial blood pressure
Time Frame
baseline and 2 hours post-dose
Title
Area under the plasma concentration versus time curve (AUC) of sildenafil
Time Frame
0, 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 16, 20, and 24 hours post-dose
Secondary Outcome Measure Information:
Title
Area under the cerebral spinal fluid concentration versus time curve (AUC) of sildenafil
Time Frame
0, 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 16, 20, and 24 hours post-dose
Title
Change from baseline in cerebral autoregulation
Time Frame
baseline and 2 hours post-dose
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age >= 21
Onset of symptoms within 72 hours from presentation
Subarachnoid hemorrhage from ruptured cerebral aneurysm
Cerebral vasospasm diagnosed on transcranial doppler, CT angiography, or digital subtraction angiography
Exclusion Criteria:
Pregnancy
Subarachnoid hemorrhage secondary to traumatic or mycotic aneurysm
Pre-ictal sildenafil therapy (last dose within 1 week of presentation)
Contraindications to sildenafil therapy (i.e. use of nitrates, left ventricular outflow obstruction, impaired autonomic blood pressure control)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chad W Washington, MS, MD, MPHS
Organizational Affiliation
University of Mississippi Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Mississippi Medical Center
City
Jackson
State/Province
Mississippi
ZIP/Postal Code
39216
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
26314998
Citation
Washington CW, Derdeyn CP, Dhar R, Arias EJ, Chicoine MR, Cross DT, Dacey RG Jr, Han BH, Moran CJ, Rich KM, Vellimana AK, Zipfel GJ. A Phase I proof-of-concept and safety trial of sildenafil to treat cerebral vasospasm following subarachnoid hemorrhage. J Neurosurg. 2016 Feb;124(2):318-27. doi: 10.3171/2015.2.JNS142752. Epub 2015 Aug 28.
Results Reference
background
PubMed Identifier
26940913
Citation
Dhar R, Washington C, Diringer M, Zazulia A, Jafri H, Derdeyn C, Zipfel G. Acute Effect of Intravenous Sildenafil on Cerebral Blood Flow in Patients with Vasospasm After Subarachnoid Hemorrhage. Neurocrit Care. 2016 Oct;25(2):201-4. doi: 10.1007/s12028-016-0243-0.
Results Reference
background
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Sildenafil for DCI
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