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Safety Study of Nicardipine to Treat Cerebral Vasospasm

Primary Purpose

Cerebral Vasospasm

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Nicardipine hydrochloride
Preservative-free normal saline
Sponsored by
University of Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Vasospasm focused on measuring Vasospasm, Subarachnoid hemorrhage, Aneurysmal subarachnoid hemorrhage, Nicardipine, Intrathecal, SAH, aSAH

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or female 18 years of age and older
  • Subarachnoid hemorrhage documented on head CT
  • Fisher Grade 3 or 4
  • Hunt Hess Grade 1-5
  • Cerebral aneurysm as definitive source of subarachnoid hemorrhage
  • Cerebral aneurysm must be treated via open or endovascular techniques
  • Presence of external ventricular drain
  • Written informed consent obtained from subject or subject's legally authorized representative

Exclusion Criteria:

  • Absence or inability to have an external ventricular drain (coagulopathy)
  • Non-aneurysmal subarachnoid hemorrhage (perimesencephalic)
  • Untreated cerebral aneurysm
  • Inability to be randomized prior to post-hemorrhage day 4
  • Elevated intra-cranial pressures that would preclude external ventricular drain clamping for 30-60 minutes
  • Inability to administer study medication (severe intra-ventricular hemorrhage, occluded external ventricular drain)
  • Inability to obtain angiography (coagulopathy, renal failure)
  • Pregnant
  • Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data

Sites / Locations

  • University of Florida

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Nicardipine hydrochloride

Preservative-free normal saline

Arm Description

Nicardipine hydrochloride 4mg by intrathecal administration twice a day until post-hemorrhage day 10.

Preservative-free normal saline 1.6 mL by intrathecal administration twice a day until post-hemorrhage day 10.

Outcomes

Primary Outcome Measures

Number of Participants With Bacterial Meningitis.

Secondary Outcome Measures

Number of Participants With Cerebral Vasospasm.

Full Information

First Posted
March 11, 2013
Last Updated
August 18, 2014
Sponsor
University of Florida
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1. Study Identification

Unique Protocol Identification Number
NCT01810302
Brief Title
Safety Study of Nicardipine to Treat Cerebral Vasospasm
Official Title
Intraventricular Nicardipine for the Treatment of Cerebral Vasospasm: Prospective Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2014
Overall Recruitment Status
Terminated
Why Stopped
Unable to secure drug.
Study Start Date
August 2013 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Florida

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if intrathecal nicardipine is safe for the treatment of cerebral vasospasm.
Detailed Description
Subarachnoid hemorrhage accounts for approximately 5% of all strokes and affects 30,000 Americans per year. Poor outcome from aneurysmal subarachnoid hemorrhage (SAH) occurs in 50 to 75% of patients, and this is attributed to secondary ischemia in approximately 30% of patients. This delayed cerebral ischemia has been attributed to the anatomic narrowing of arteries in the cerebral vasculature which occurs following SAH. Because of this relationship between cerebral vasospasm, cerebral ischemia, and poor outcome, there has been significant effort to establish treatments that decrease the incidence of vasospasm after SAH. Currently, medications and hemodynamic maneuvers are used as standard of care for the treatment of vasospasm and to improve outcome after SAH. The calcium channel blocker, nimodipine, is one of the few treatments for vasospasm that has been shown to be of proven benefit. Nicardipine is another calcium channel blocker that has been evaluated in several studies via an intravenous administration route. These studies did show significant improvements in symptomatic and angiographic vasospasm, although a benefit in outcome was not seen. However, the intravenous administration of nicardipine was associated with significant systemic side effects that may have affected outcome including hypotension, pulmonary edema, and azotemia. The administration of nicardipine via an intrathecal route avoids the systemic complications associated with intravenous dosing since the direct cerebrospinal fluid dosing is much lower. The result is that the systemic concentration will remain low avoiding systemic side effects, and central nervous system concentration will remain high. We propose that this difference may improve outcomes while minimizing complication related effects on patient outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Vasospasm
Keywords
Vasospasm, Subarachnoid hemorrhage, Aneurysmal subarachnoid hemorrhage, Nicardipine, Intrathecal, SAH, aSAH

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Nicardipine hydrochloride
Arm Type
Experimental
Arm Description
Nicardipine hydrochloride 4mg by intrathecal administration twice a day until post-hemorrhage day 10.
Arm Title
Preservative-free normal saline
Arm Type
Placebo Comparator
Arm Description
Preservative-free normal saline 1.6 mL by intrathecal administration twice a day until post-hemorrhage day 10.
Intervention Type
Drug
Intervention Name(s)
Nicardipine hydrochloride
Other Intervention Name(s)
Nicardipine, Cardene
Intervention Description
Nicardipine hydrochloride 4mg by intrathecal administration twice a day until post-hemorrhage day 10.
Intervention Type
Drug
Intervention Name(s)
Preservative-free normal saline
Other Intervention Name(s)
Normal saline, Placebo, NS
Intervention Description
Preservative-free normal saline 1.6 mL by intrathecal administration twice a day until post-hemorrhage day 10.
Primary Outcome Measure Information:
Title
Number of Participants With Bacterial Meningitis.
Time Frame
Day 1 of study drug until post-hemorrhage day 10.
Secondary Outcome Measure Information:
Title
Number of Participants With Cerebral Vasospasm.
Time Frame
Day 1 of study drug until post-hemorrhage day 10.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female 18 years of age and older Subarachnoid hemorrhage documented on head CT Fisher Grade 3 or 4 Hunt Hess Grade 1-5 Cerebral aneurysm as definitive source of subarachnoid hemorrhage Cerebral aneurysm must be treated via open or endovascular techniques Presence of external ventricular drain Written informed consent obtained from subject or subject's legally authorized representative Exclusion Criteria: Absence or inability to have an external ventricular drain (coagulopathy) Non-aneurysmal subarachnoid hemorrhage (perimesencephalic) Untreated cerebral aneurysm Inability to be randomized prior to post-hemorrhage day 4 Elevated intra-cranial pressures that would preclude external ventricular drain clamping for 30-60 minutes Inability to administer study medication (severe intra-ventricular hemorrhage, occluded external ventricular drain) Inability to obtain angiography (coagulopathy, renal failure) Pregnant Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Spiros L. Blackburn, MD
Organizational Affiliation
University of Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Florida
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32610
Country
United States

12. IPD Sharing Statement

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Safety Study of Nicardipine to Treat Cerebral Vasospasm

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