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Efficacy and Safety of Factor VIIa on Rebleeding After Surgery for Spontaneous Intracerebral Hemorrhage (ICH) (PRE-SICH)

Primary Purpose

Intracerebral Hemorrhage

Status
Completed
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
rFactor VIIa (Eptacog alfa, NovoNordisk)
rFVIIa
Sodiun chloride 0.9%
Sponsored by
IRCCS Policlinico S. Matteo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Intracerebral Hemorrhage focused on measuring Spontaneous intracerebral hemorrhage, ICH, intracerebral rebleeding, cerebral hematoma evacuation, cerebral hematoma volume

Eligibility Criteria

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

Inclusion Criteria: Male or female, aged 18-75 years inclusive Intraparenchymal primary supratentorial intracerebral hemorrhage requiring surgical evacuation Any Glasgow Coma Score (GCS) score Surgery expected to be performed within 24 hours from symptoms onset Exclusion Criteria: Age below 18 Intraparenchymal hematoma secondary to rupture of cerebral aneurysm or bleeding of arteriovenous (A-V) malformation or cerebral tumors Contemporary involvement in another study Pregnancy Myocardial infarction in the six months preceding enrolment Coronary or carotid stents positioned in the six months preceding enrolment Solid organ transplant patients (e.g., heart, lung, liver, kidney) Pregnancy Myocardial infarction in the six months preceding enrolment Coronary and carotid stents positioned in the six months preceding enrolment Solid organ transplant patients (e.g., heart, lung, liver, kidney)

Sites / Locations

  • Azienda Ospedaliera S. Croce e Carle
  • Azienda Ospedaliera "Maggiore della Carità"
  • II Dpt Anesthesiology&Critical Care Medicine - IRCCS Policlinico S. Matteo

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

1

2

Arm Description

Patients treated with recombinant FVIIa

Patients with spontaneous supratentorial ICH included in this arm will be treated with placebo

Outcomes

Primary Outcome Measures

Evaluate the efficacy of Factor VIIa (Eptacog alfa) in preventing or reducing rebleeding after surgery for spontaneous supratentorial ICH

Secondary Outcome Measures

Safety of product administration

Full Information

First Posted
August 8, 2005
Last Updated
February 3, 2009
Sponsor
IRCCS Policlinico S. Matteo
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1. Study Identification

Unique Protocol Identification Number
NCT00128050
Brief Title
Efficacy and Safety of Factor VIIa on Rebleeding After Surgery for Spontaneous Intracerebral Hemorrhage (ICH)
Acronym
PRE-SICH
Official Title
Efficacy and Safety of Factor VIIa (Eptacog Alfa) on Rebleeding After Surgery for Spontaneous Supratentorial Intracerebral Hemorrhage. A Randomized, Controlled, Open-Label, Investigator-Blinded Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
IRCCS Policlinico S. Matteo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Although the role of surgical treatment is still controversial, surgical evacuation of intracerebral hematoma is a frequent practice. Rebleeding is a frequent complication in patients submitted to hematoma evacuation. It has been reported that smaller postoperative volume of hematoma is associated with a better outcome. The investigators hypothesize that the administration of Factor VIIa (Eptacog alfa) immediately after surgical evacuation of the hematoma can reduce postoperative rebleeding. Aims of the Study: This study will investigate: The efficacy of Eptacog alfa in preventing or reducing rebleeding after surgery for spontaneous supratentorial ICH; and The safety of product administration
Detailed Description
The primary endpoint is the evaluation of efficacy of Factor VIIa (Eptacog alfa, NovoSeven, Novo Nordisk) on rebleeding after surgery for primary supratentorial ICH. All patients included in the study will perform a CT scan within 3 hours before surgery, then immediately after surgery, and 18-30 hours after surgery. The hematoma volume will be evaluated by a multi-slice CT scan. All CT scan images will be sent to the Coordinating Center where the hematoma volume will be evaluated by a dedicated software by the same investigator who will be unaware of the treatment (investigator- blinded study). SAFETY EVALUATION: Seventeen episodes of thrombotic spontaneous adverse events have been reported after administration of 480,000 standard doses of Eptacog alfa in hemophilic patients. These episodes include myocardial infarction, acute cerebrovascular thrombosis, disseminated intravascular coagulation (DIC), deep venous thrombosis (DVT) and pulmonary embolism. Before and after hematoma removal will be evaluated ECG, myocardiac enzymes, coagulation profile, CT scan (looking for ischemic events) and venous echodoppler ultrasound of lower extremities.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intracerebral Hemorrhage
Keywords
Spontaneous intracerebral hemorrhage, ICH, intracerebral rebleeding, cerebral hematoma evacuation, cerebral hematoma volume

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Patients treated with recombinant FVIIa
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Patients with spontaneous supratentorial ICH included in this arm will be treated with placebo
Intervention Type
Drug
Intervention Name(s)
rFactor VIIa (Eptacog alfa, NovoNordisk)
Intervention Description
rFVIIa will be admistered as single bolus at the dosage of 100 mcg/Kg b.w.
Intervention Type
Drug
Intervention Name(s)
rFVIIa
Intervention Description
Patients with spontaneous supratentorial ICH will be treated with rFVII after hematoma evacuation
Intervention Type
Other
Intervention Name(s)
Sodiun chloride 0.9%
Intervention Description
Bolus injection of sodium chloride 0.9% after surgical hematoma removal
Primary Outcome Measure Information:
Title
Evaluate the efficacy of Factor VIIa (Eptacog alfa) in preventing or reducing rebleeding after surgery for spontaneous supratentorial ICH
Time Frame
4 years
Secondary Outcome Measure Information:
Title
Safety of product administration
Time Frame
4 years

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: Male or female, aged 18-75 years inclusive Intraparenchymal primary supratentorial intracerebral hemorrhage requiring surgical evacuation Any Glasgow Coma Score (GCS) score Surgery expected to be performed within 24 hours from symptoms onset Exclusion Criteria: Age below 18 Intraparenchymal hematoma secondary to rupture of cerebral aneurysm or bleeding of arteriovenous (A-V) malformation or cerebral tumors Contemporary involvement in another study Pregnancy Myocardial infarction in the six months preceding enrolment Coronary or carotid stents positioned in the six months preceding enrolment Solid organ transplant patients (e.g., heart, lung, liver, kidney) Pregnancy Myocardial infarction in the six months preceding enrolment Coronary and carotid stents positioned in the six months preceding enrolment Solid organ transplant patients (e.g., heart, lung, liver, kidney)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roberto Imberti, M.D.
Organizational Affiliation
IRCCS Policlinico S. Matteo - Pavia - Italy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Azienda Ospedaliera S. Croce e Carle
City
Cuneo
ZIP/Postal Code
12100
Country
Italy
Facility Name
Azienda Ospedaliera "Maggiore della Carità"
City
Novara
ZIP/Postal Code
28100
Country
Italy
Facility Name
II Dpt Anesthesiology&Critical Care Medicine - IRCCS Policlinico S. Matteo
City
Pavia
ZIP/Postal Code
27100
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
11376176
Citation
Morgenstern LB, Demchuk AM, Kim DH, Frankowski RF, Grotta JC. Rebleeding leads to poor outcome in ultra-early craniotomy for intracerebral hemorrhage. Neurology. 2001 May 22;56(10):1294-9. doi: 10.1212/wnl.56.10.1294.
Results Reference
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Efficacy and Safety of Factor VIIa on Rebleeding After Surgery for Spontaneous Intracerebral Hemorrhage (ICH)

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