Intraventricular Tissue Plasminogen Activator (tPA) in the Management of Aneurysmal Subarachnoid Hemorrhage

• Status: Unknown status
• Trial end date: 2012-04-01
• Target enrollment: 0
• Participant gender: All

Summary

The proposed study is to evaluate the acceleration the clearance of intraventricular blood (IVH) and subarachnoid hemorrhage (SAH) following ruptured intracranial aneurysms, thereby ameliorating complications, such as cerebral vasospasm, hydrocephalus and intracranial hypertension.

The primary objectives are:

1. Estimate the rate and variance of hematoma clearance following aneurysmal SAH, thereby facilitating sample size determination for a subsequent larger study;

2. Assess the feasibility of a randomized controlled trial of intraventricular tissue plasminogen activator (TPA) among patients with SAH (enrollment rate, ability to blind investigators, protocol compliance);

3. Confirm the safety of intraventricular TPA.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University of Calgary
• Treatments: Plasminogen; Tissue Plasminogen Activator

Criteria

Inclusion Criteria:

• Adult patients (> 18 years old) with a proven ruptured cerebral aneurysm

• Aneurysm has been / will be treated with coil embolization

• EVD has been / will be placed as part of routine care

• Modified Fisher score is 4 (cisternal blood > 1 mm thick with concomitant IVH)

• CT scan after EVD placement shows "stability" with no increase in the amount of intracranial blood (Note: there is sometimes layering of blood, especially in the occipital horns of the lateral ventricles, that develops during the first 24-48 hours after a ruptured aneurysm due to circulation of blood in the CSF - this does not necessarily constitute an exclusion criterion).

• Study drug can be administered within 72 hours of the time of SAH.

Exclusion Criteria:

• Concern expressed by endovascular neurosurgeon / interventional radiologist that aneurysm has only been incompletely treated / isolated by coil embolization.

• Patient requires craniotomy and clipping of the culprit aneurysm.

• CT scan performed post-EVD insertion OR post-coiling shows increase in amount of intracranial blood.

• Uncorrected coagulation disturbance (INR > 1.5, PTT > 45); correction is permitted (if coagulation disturbance develops during the study, subsequent doses of TPA should simply be withheld until coagulation can be corrected).

• Uncorrected thrombocytopenia (platelets < 50,000); correction with platelet transfusions is permitted.

• Involvement in another clinical trial

• Uncontrolled active internal hemorrhage

• Known allergy to study drug

• Patient is pregnant

• Any other condition the investigator believes would place the subject at risk if included in the study.