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Sonothrombolysis Potentiated by Microbubbles for Acute Ischemic Stroke

Primary Purpose

Cerebrovascular Stroke

Status
Completed
Phase
Phase 2
Locations
Spain
Study Type
Interventional
Intervention
Sulfur hexafluoride + ultrasounds
Recombinant tissue plasminogen activator
Sponsored by
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebrovascular Stroke

Eligibility Criteria

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

Inclusion Criteria:

  • All acute (<4,5 hours) ischemic stroke patients in the MCA territory (as depicted by head computed tomography CT or suspected by clinical data) with a disabling neurological deficit measurable by National Institute of Health Stroke Scale (NIHSS) score, that in the opinion of treating physicians require and meet accepted criteria of treatment with a standard 0.9 mg/kg dose of iv rtPA.
  • A documented occlusion of the middle cerebral artery (MCA) documented by TCD and/or angioCT.
  • The patient or the legal representative signs the written consent to participate
  • Age > or = 18 years
  • No significant improvement before treatment.
  • The treatment is initiated within 90 minutes of hospital admission (door-to-needle time < or = 90 minutes)
  • There is no limitation regarding the NIHSS score. Scores under 5 are usually considered mild strokes, but they can be treated if the investigator believes that the measured deficit is important enough to cause disability. The investigator should weight benefits and risks when the score is under 5 and above 22.

Exclusion Criteria:

  • severe stroke as indicated on baseline CT imaging or by a NIHSS score > 25
  • evidence of hemorrhage on noncontrast head computed tomography CT),
  • any other standard contraindication for intravenous rtPA therapy,
  • primary treatment with intra-arterial thrombolysis,
  • Previous Rankin scale score > 1 and NIHSS < 14 or previous Rankin scale score > 2 and NIHSS > or = 14
  • Rapidly improving neurological symptoms such that the rate of improvement is expected to result in a NIHSS score of < 4 at randomization
  • Coexisting neurological diseases such as dementia or life-threatening illness.
  • Seizure at symptom onset
  • History or clinical presentation of intracranial hemorrhage, subarachnoid hemorrhage (even with a normal CT), arteriovenous malformation, aneurysm, spinal cord disease or cerebral neoplasm. Incidental meningioma and microbleeds per se are not exclusion criteria.
  • Baseline blood glucose concentration less than 50 mg/dL or greater than 400 mg/dl, that cannot be corrected
  • Uncontrolled hypertension, defined as systolic blood pressure > 185 mm Hg or diastolic blood pressure > 110 mm Hg on at least two separate occasions at least 10 min apart, or blood pressure that requires aggressive treatment to reduce it to within these limits
  • Hereditary or acquired hemorrhagic diathesis
  • Another stroke, a serious head injury or major surgery within the previous 3 month
  • Platelet count < 100.000/mm3
  • Hemorrhagic retinopathy
  • Within 10 days of traumatic external heart massage, obstetrical delivery, recent puncture of a non-compressible blood-vessel
  • Bacterial endocarditis, pericarditis
  • Acute pancreatitis; documented ulcerative gastrointestinal disease during the last 3 months, esophageal varices
  • Arterial aneurysm, arterial/venous malformations
  • Neoplasm with increased bleeding risk
  • Severe liver disease, including hepatic failure, cirrhosis, portal hypertension and active hepatitis
  • Major surgery or significant trauma in past 3 months
  • Contraindication to CT perfusion: Iodinated contrast allergy, renal insufficiency (elevated serum creatinine above normal laboratory levels at each center), non-collaborative patients, pregnancy

Sites / Locations

  • Hospital de la Santa Creu i Sant Pau

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Sonothrombolysis + microbubbles

Standard intravenous thrombolysis

Arm Description

rtPA+ sonovue. SonoVue sulphur hexafluoride microbubbles 8 microlitres/ml Powder and solvent for dispersion for injection 1 vial containing 25 mg lyophilized powder to be reconstituted with 5 ml sodium chloride 9 mg/ml (0.9%) solution for injection 1 pre-filled syringe containing sodium chloride 9 mg/ml (0.9%) solution for injection 1 Mini-Spike Plus 6/8 (CE 0123) transfer system. 1 ml of the reconstituted dispersion contains 8 microlitres sulphur hexafluoride microbubbles.

Patients in thecontrol group will use thehelmetbut without U.S continuous U.S wave emission. Serial monitoring of the status ofrecanalizationaccording to theschedule set will be carried out according to theestablished schedule

Outcomes

Primary Outcome Measures

Recanalization rate
The short term efficacy of treatment will be evaluated by recanalization rate at 6 hours control TCD (TIBI score) and at 24 hours by the NIHSS (a > 4 points improvement). As explained, the Rankin scale score will be used to test the efficacy of the treatment at day 90 after stroke onset.

Secondary Outcome Measures

Full Information

First Posted
August 31, 2012
Last Updated
August 7, 2015
Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
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1. Study Identification

Unique Protocol Identification Number
NCT01678495
Brief Title
Sonothrombolysis Potentiated by Microbubbles for Acute Ischemic Stroke
Official Title
Sonothrombolysis Potentiated by Microbubbles as a Novel Treatment of Acute Ischemic Stroke: a Prospective Randomized Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
August 2012 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
July 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
It has proposed the use of ST without microbubble treatment in randomized association with both intravenous and intra-arterial thrombolysis, but combined treatment (rtPA + U.S.) associated with MB diagnostic not yet been investigated in a randomized study. The aim of this study is to evaluate efficacy of the combined treatment (r-rtPA+US+MB) vs the standard rtPA treatment in a randomized study in consecutive patients with acute ischemic stroke. We expect to demonstrate that the combined treatment (rtPA+US+MB) will be statistically superior to standard treatment in terms of recanalization rate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebrovascular Stroke

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Sonothrombolysis + microbubbles
Arm Type
Experimental
Arm Description
rtPA+ sonovue. SonoVue sulphur hexafluoride microbubbles 8 microlitres/ml Powder and solvent for dispersion for injection 1 vial containing 25 mg lyophilized powder to be reconstituted with 5 ml sodium chloride 9 mg/ml (0.9%) solution for injection 1 pre-filled syringe containing sodium chloride 9 mg/ml (0.9%) solution for injection 1 Mini-Spike Plus 6/8 (CE 0123) transfer system. 1 ml of the reconstituted dispersion contains 8 microlitres sulphur hexafluoride microbubbles.
Arm Title
Standard intravenous thrombolysis
Arm Type
Active Comparator
Arm Description
Patients in thecontrol group will use thehelmetbut without U.S continuous U.S wave emission. Serial monitoring of the status ofrecanalizationaccording to theschedule set will be carried out according to theestablished schedule
Intervention Type
Other
Intervention Name(s)
Sulfur hexafluoride + ultrasounds
Intervention Type
Drug
Intervention Name(s)
Recombinant tissue plasminogen activator
Primary Outcome Measure Information:
Title
Recanalization rate
Description
The short term efficacy of treatment will be evaluated by recanalization rate at 6 hours control TCD (TIBI score) and at 24 hours by the NIHSS (a > 4 points improvement). As explained, the Rankin scale score will be used to test the efficacy of the treatment at day 90 after stroke onset.
Time Frame
6 h, 24h, and day 90 post treatmente

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All acute (<4,5 hours) ischemic stroke patients in the MCA territory (as depicted by head computed tomography CT or suspected by clinical data) with a disabling neurological deficit measurable by National Institute of Health Stroke Scale (NIHSS) score, that in the opinion of treating physicians require and meet accepted criteria of treatment with a standard 0.9 mg/kg dose of iv rtPA. A documented occlusion of the middle cerebral artery (MCA) documented by TCD and/or angioCT. The patient or the legal representative signs the written consent to participate Age > or = 18 years No significant improvement before treatment. The treatment is initiated within 90 minutes of hospital admission (door-to-needle time < or = 90 minutes) There is no limitation regarding the NIHSS score. Scores under 5 are usually considered mild strokes, but they can be treated if the investigator believes that the measured deficit is important enough to cause disability. The investigator should weight benefits and risks when the score is under 5 and above 22. Exclusion Criteria: severe stroke as indicated on baseline CT imaging or by a NIHSS score > 25 evidence of hemorrhage on noncontrast head computed tomography CT), any other standard contraindication for intravenous rtPA therapy, primary treatment with intra-arterial thrombolysis, Previous Rankin scale score > 1 and NIHSS < 14 or previous Rankin scale score > 2 and NIHSS > or = 14 Rapidly improving neurological symptoms such that the rate of improvement is expected to result in a NIHSS score of < 4 at randomization Coexisting neurological diseases such as dementia or life-threatening illness. Seizure at symptom onset History or clinical presentation of intracranial hemorrhage, subarachnoid hemorrhage (even with a normal CT), arteriovenous malformation, aneurysm, spinal cord disease or cerebral neoplasm. Incidental meningioma and microbleeds per se are not exclusion criteria. Baseline blood glucose concentration less than 50 mg/dL or greater than 400 mg/dl, that cannot be corrected Uncontrolled hypertension, defined as systolic blood pressure > 185 mm Hg or diastolic blood pressure > 110 mm Hg on at least two separate occasions at least 10 min apart, or blood pressure that requires aggressive treatment to reduce it to within these limits Hereditary or acquired hemorrhagic diathesis Another stroke, a serious head injury or major surgery within the previous 3 month Platelet count < 100.000/mm3 Hemorrhagic retinopathy Within 10 days of traumatic external heart massage, obstetrical delivery, recent puncture of a non-compressible blood-vessel Bacterial endocarditis, pericarditis Acute pancreatitis; documented ulcerative gastrointestinal disease during the last 3 months, esophageal varices Arterial aneurysm, arterial/venous malformations Neoplasm with increased bleeding risk Severe liver disease, including hepatic failure, cirrhosis, portal hypertension and active hepatitis Major surgery or significant trauma in past 3 months Contraindication to CT perfusion: Iodinated contrast allergy, renal insufficiency (elevated serum creatinine above normal laboratory levels at each center), non-collaborative patients, pregnancy
Facility Information:
Facility Name
Hospital de la Santa Creu i Sant Pau
City
Barcelona
ZIP/Postal Code
08025
Country
Spain

12. IPD Sharing Statement

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Sonothrombolysis Potentiated by Microbubbles for Acute Ischemic Stroke

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