search
Back to results

Intraventricular Rt-PA in Patients With Intraventricular Hemorrhage

Primary Purpose

Cerebral Hemorrhage

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Recombinant Tissue Plasminogen Activator (rt-PA)
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Hemorrhage focused on measuring Intraventricular hemorrhage, Subarachnoid hemorrhage, Intracerebral hemorrhage, Pharmacokinetics, Recombinant Proteins, Anticoagulants, Tissue Plasminogen Activator, Pharmacology, Catheters, Indwelling, Cerebral Ventricles

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria: Intraventricular hemorrhage (IVH) confirmed by CT scan More than 12 hours post bleed Hematoma size stable by CT scan Post-IVH catheter CT scan Able to begin study within 24 hours of bleed Exclusion criteria: Infratentorial bleed Supratentorial bleed greater than 30 cc Unclipped aneurysm suspected Arteriovenous malformation suspected Any severe, complicating illness (e.g., AIDS or DNR) Cardiovascular parameters that could confound study (e.g., myocardial infarction, pulmonary emboli, systemic fibrinolysis) Active internal bleeding Requirement for heparin doses greater than 10,000 U/day Concurrent coumadin Known allergy to rt-PA Pregnancy

Sites / Locations

  • The Johns Hopkins University

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
January 10, 2002
Last Updated
March 24, 2015
Sponsor
Johns Hopkins University
search

1. Study Identification

Unique Protocol Identification Number
NCT00029315
Brief Title
Intraventricular Rt-PA in Patients With Intraventricular Hemorrhage
Official Title
Intraventricular Rt-PA Pharmacokinetic and Pharmacodynamic Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2001
Overall Recruitment Status
Completed
Study Start Date
September 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2004 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Johns Hopkins University

4. Oversight

5. Study Description

Brief Summary
This is a study to evaluate how recombinant tissue plasminogen activator (rt-PA) is utilized in patients with intraventricular hemorrhage (IVH). rt-PA is a drug that has been shown to dissolve blood, and may allow intraventricular catheters to be more effective for a longer period of time.
Detailed Description
IVH occurs in about 40 percent of intracerebral hemorrhage cases and 15 percent of aneurysmal subarachnoid hemorrhage cases. Evidence supports a strong contribution of IVH to morbidity and mortality after cerebral hemorrhage. External ventricular drainage (EVD) is required clinical management; however, EVD via intraventricular catheter alone fails to prevent much of the morbidity and mortality of IVH. This study seeks to demonstrate the safety and efficacy of intraventricular thrombolysis, using rt-PA, as a method of removing this blood and altering morbidity and mortality. Patients will receive intraventricular injections of rt-PA or placebo every 12 hours. They will be followed prospectively with daily head CT scans during the acute-treatment phase and again between Days 28 and 32. Completion date provided represents the completion date of the grant per OOPD records

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Hemorrhage
Keywords
Intraventricular hemorrhage, Subarachnoid hemorrhage, Intracerebral hemorrhage, Pharmacokinetics, Recombinant Proteins, Anticoagulants, Tissue Plasminogen Activator, Pharmacology, Catheters, Indwelling, Cerebral Ventricles

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Masking
Double
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Recombinant Tissue Plasminogen Activator (rt-PA)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Intraventricular hemorrhage (IVH) confirmed by CT scan More than 12 hours post bleed Hematoma size stable by CT scan Post-IVH catheter CT scan Able to begin study within 24 hours of bleed Exclusion criteria: Infratentorial bleed Supratentorial bleed greater than 30 cc Unclipped aneurysm suspected Arteriovenous malformation suspected Any severe, complicating illness (e.g., AIDS or DNR) Cardiovascular parameters that could confound study (e.g., myocardial infarction, pulmonary emboli, systemic fibrinolysis) Active internal bleeding Requirement for heparin doses greater than 10,000 U/day Concurrent coumadin Known allergy to rt-PA Pregnancy
Facility Information:
Facility Name
The Johns Hopkins University
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Intraventricular Rt-PA in Patients With Intraventricular Hemorrhage

We'll reach out to this number within 24 hrs