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Vitamin K1 in the Treatment of Spontaneous Intracerebral Hemorrhage

Primary Purpose

Intracerebral Haemorrhage in Cerebellum

Status
Unknown status
Phase
Early Phase 1
Locations
China
Study Type
Interventional
Intervention
Vitamin K 1
normal saline
Sponsored by
HUANG XIANJIAN
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Intracerebral Haemorrhage in Cerebellum focused on measuring vitamin K1, spontaneous intracerebral hemorrhage, effectiveness, outcome

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Spontaneous intracerebral hemorrhage (Non - aneurysmal or arteriovenous malformations which confirmed by cerebral arterial CT enhancement or DSA);
  • Age 18-65 years, male or non-pregnant female;
  • GCS score at admission (4 to12);
  • during the hospitalization, no urokinase and other hemostatic drugs were used except for etamsylate and vitamin K1;
  • informed consent signed by the patient's family

Exclusion Criteria:

  • irregular lobulated hematoma (volume of hematoma can not be calculated accurately), such as intraventricular hemorrhage;
  • severe liver disease or impaired liver function;
  • pregnant or lactating women;
  • history of using anticoagulation or antiplatelet aggregation drug (including Cilostazol, aspirin, dipyridamole, heparin, low molecular weight heparin, hirudin, dabigatran, and warfarin);
  • non-accepted informed consent

Sites / Locations

  • Shenzhen second people's hospital
  • The fifth people's hospital of Longgang District, Shenzhen
  • Baoan District central hospital of Shenzhen
  • Shajing hospital of Baoan District ,Shenzhen
  • The second People's hospital of Longgang District, Shenzhen

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

research group

placebo group

Arm Description

normal saline 100ml+ vitamin K1 20mg ivgtt qd day0 and day1。

normal saline100ml + normal saline 2 ml ivgtt qd day0 and day1

Outcomes

Primary Outcome Measures

The volume of cerebral hemorrhage
The volume of cerebral hemorrhage at certain time post onset(ml)
The volume of cerebral hemorrhage
The volume of cerebral hemorrhage at certain time post onset(ml)
The volume of cerebral hemorrhage
The volume of cerebral hemorrhage at certain time post onset(ml)

Secondary Outcome Measures

The Activated Partial Thromboplastin Time(s)at certain time post onset
Activated Partial Thromboplastin Time(s)
The Activated Partial Thromboplastin Time(s)at certain time post onset
Activated Partial Thromboplastin Time(s)
The Activated Partial Thromboplastin Time(s)at certain time post onset
Activated Partial Thromboplastin Time(s)
The condition of Platelet level at certain time post onset
The condition of Platelet level at certain time post onset(10^9/L)
The condition of Platelet level at certain time post onset
The condition of Platelet level at certain time post onset(10^9/L)
The condition of Platelet level at certain time post onset
The condition of Platelet level at certain time post onset(10^9/L)
The condition of GCS scale post(3-15) at certain time post onset
The condition of GCS scale post(3-15) at certain time post onset
The condition of GCS scale post(3-15) at certain time post onset
The condition of GCS scale post(3-15) at certain time post onset
The condition of GCS scale post(3-15) at certain time post onset
The condition of GCS scale post(3-15) at certain time post onset
The prothrombin time(s) at certain time post onset
prothrombin time(s)
The prothrombin time(s) at certain time post onset
prothrombin time(s)
The prothrombin time(s) at certain time post onset
prothrombin time(s)
The Fibrinogen (g/L)at certain time post onset
Fibrinogen (g/L)
The Fibrinogen (g/L)at certain time post onset
Fibrinogen (g/L)
The Fibrinogen (g/L)at certain time post onset
Fibrinogen (g/L)
The Thrombin Time(s) at certain time post onset
Thrombin Time(s)
The Thrombin Time(s) at certain time post onset
Thrombin Time(s)
The Thrombin Time(s) at certain time post onset
Thrombin Time(s)

Full Information

First Posted
October 29, 2017
Last Updated
January 3, 2018
Sponsor
HUANG XIANJIAN
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1. Study Identification

Unique Protocol Identification Number
NCT03388970
Brief Title
Vitamin K1 in the Treatment of Spontaneous Intracerebral Hemorrhage
Official Title
Multicenter Randomized Controlled Trial of Vitamin K1 in the Treatment of Spontaneous Intracerebral Hemorrhage
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2017 (Actual)
Primary Completion Date
October 31, 2018 (Anticipated)
Study Completion Date
July 1, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
HUANG XIANJIAN

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
In order to determine the effectiveness and safety of early vitamin K1 use in reducing the risk of bleeding and improving prognosis in patients with spontaneous intracerebral hemorrhage. Patients with spontaneous intracerebral hemorrhage (excluding rupture of aneurysm and vascular malformation) will be randomly divided into experimental group and control group. All the patients in the two groups were treated according to the guideline of spontaneous intracerebral hemorrhage. Patients in the experimental group was treated with intravenous injection of vitamin K1 20mg once a day for 2 days after admission, and the patients in control group was treated with normal saline as a control. The hematoma volume, coagulation function, platelet levels and GCS scales of the two groups will be recorded in 0d, 1d, 3d, 7d post bleeding stroke, furthermore, length of ICU stay and total hospitalization, incidence of complications during hospitalization are to be recorded. During the follow-up, mRS score will be recorded at 1m and 6m post bleeding stroke.
Detailed Description
Spontaneous intracerebral hemorrhage is a common disease in the department of neurosurgery, which often leads to long-term coma and severe neurological dysfunction. The amount of cerebral hemorrhage is directly related to the prognosis of the patients, and a small number of patients still suffer from the adverse consequences of delayed bleeding after active treatment. Vitamin K1 is a necessary ingredient in the liver to produce clotting factors II, VII, IX, and X, and vitamin K1 supplementation increases clotting function. On the contrary, vitamin K1 increases the risk of thrombosis. In this study, patients with spontaneous intracerebral hemorrhage (excluding rupture of aneurysm and vascular malformation) will be randomly divided into experimental group and control group. All the patients in the two groups were treated according to the guideline of spontaneous intracerebral hemorrhage. Patients in the experimental group was treated with intravenous injection of vitamin K1 20mg once a day for 2 days after admission, and the patients in control group was treated with normal saline as a control. The hematoma volume, coagulation function, platelet levels and GCS scales of the two groups will be recorded in 0d, 1d, 3d, 7d post bleeding stroke, furthermore, length of ICU stay and total hospitalization, incidence of complications during hospitalization are to be recorded. During the follow-up, mRS score will be recorded at 1m and 6m post bleeding stroke. Finally, the effectiveness and safety of early vitamin K1 use in reducing the risk of bleeding and improving prognosis in patients with spontaneous intracerebral hemorrhage will be analyzed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intracerebral Haemorrhage in Cerebellum
Keywords
vitamin K1, spontaneous intracerebral hemorrhage, effectiveness, outcome

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
patient and family members
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
research group
Arm Type
Experimental
Arm Description
normal saline 100ml+ vitamin K1 20mg ivgtt qd day0 and day1。
Arm Title
placebo group
Arm Type
Placebo Comparator
Arm Description
normal saline100ml + normal saline 2 ml ivgtt qd day0 and day1
Intervention Type
Drug
Intervention Name(s)
Vitamin K 1
Intervention Description
Research group use Vitamin K1
Intervention Type
Drug
Intervention Name(s)
normal saline
Intervention Description
Placebo group use normal saline
Primary Outcome Measure Information:
Title
The volume of cerebral hemorrhage
Description
The volume of cerebral hemorrhage at certain time post onset(ml)
Time Frame
Day0
Title
The volume of cerebral hemorrhage
Description
The volume of cerebral hemorrhage at certain time post onset(ml)
Time Frame
Day3
Title
The volume of cerebral hemorrhage
Description
The volume of cerebral hemorrhage at certain time post onset(ml)
Time Frame
Day7
Secondary Outcome Measure Information:
Title
The Activated Partial Thromboplastin Time(s)at certain time post onset
Description
Activated Partial Thromboplastin Time(s)
Time Frame
Day0
Title
The Activated Partial Thromboplastin Time(s)at certain time post onset
Description
Activated Partial Thromboplastin Time(s)
Time Frame
Day3
Title
The Activated Partial Thromboplastin Time(s)at certain time post onset
Description
Activated Partial Thromboplastin Time(s)
Time Frame
Day7
Title
The condition of Platelet level at certain time post onset
Description
The condition of Platelet level at certain time post onset(10^9/L)
Time Frame
Day0
Title
The condition of Platelet level at certain time post onset
Description
The condition of Platelet level at certain time post onset(10^9/L)
Time Frame
Day3
Title
The condition of Platelet level at certain time post onset
Description
The condition of Platelet level at certain time post onset(10^9/L)
Time Frame
Day7
Title
The condition of GCS scale post(3-15) at certain time post onset
Description
The condition of GCS scale post(3-15) at certain time post onset
Time Frame
Day0
Title
The condition of GCS scale post(3-15) at certain time post onset
Description
The condition of GCS scale post(3-15) at certain time post onset
Time Frame
Day3
Title
The condition of GCS scale post(3-15) at certain time post onset
Description
The condition of GCS scale post(3-15) at certain time post onset
Time Frame
Day7
Title
The prothrombin time(s) at certain time post onset
Description
prothrombin time(s)
Time Frame
Day0
Title
The prothrombin time(s) at certain time post onset
Description
prothrombin time(s)
Time Frame
Day3
Title
The prothrombin time(s) at certain time post onset
Description
prothrombin time(s)
Time Frame
Day7
Title
The Fibrinogen (g/L)at certain time post onset
Description
Fibrinogen (g/L)
Time Frame
Day0
Title
The Fibrinogen (g/L)at certain time post onset
Description
Fibrinogen (g/L)
Time Frame
Day3
Title
The Fibrinogen (g/L)at certain time post onset
Description
Fibrinogen (g/L)
Time Frame
Day7
Title
The Thrombin Time(s) at certain time post onset
Description
Thrombin Time(s)
Time Frame
Day0
Title
The Thrombin Time(s) at certain time post onset
Description
Thrombin Time(s)
Time Frame
Day3
Title
The Thrombin Time(s) at certain time post onset
Description
Thrombin Time(s)
Time Frame
Day7
Other Pre-specified Outcome Measures:
Title
length of stay in ICU
Description
length of stay in ICU
Time Frame
about two weeks
Title
Total hospital stay
Description
Total hospital stay
Time Frame
about one month
Title
Complications1
Description
neurologic complications
Time Frame
6 month post onset
Title
The Modified Rankin Scale (mRS)
Description
The scale runs from 0-6, running from perfect health without symptoms to death.0 - No symptoms.1 - No significant disability. Able to carry out all usual activities, despite some symptoms.2 - Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities. 3 - Moderate disability. Requires some help, but able to walk unassisted. 4 - Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted. 5 - Severe disability. Requires constant nursing care and attention, bedridden, incontinent. 6 - Dead.
Time Frame
month 1 post onset
Title
The Modified Rankin Scale (mRS)
Description
The scale runs from 0-6, running from perfect health without symptoms to death.0 - No symptoms.1 - No significant disability. Able to carry out all usual activities, despite some symptoms.2 - Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities. 3 - Moderate disability. Requires some help, but able to walk unassisted. 4 - Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted. 5 - Severe disability. Requires constant nursing care and attention, bedridden, incontinent. 6 - Dead.
Time Frame
month 6 post onset
Title
Complications2
Description
infection complications
Time Frame
6 month post onset
Title
Complications3
Description
complications of coagulation
Time Frame
6 month post onset

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Spontaneous intracerebral hemorrhage (Non - aneurysmal or arteriovenous malformations which confirmed by cerebral arterial CT enhancement or DSA); Age 18-65 years, male or non-pregnant female; GCS score at admission (4 to12); during the hospitalization, no urokinase and other hemostatic drugs were used except for etamsylate and vitamin K1; informed consent signed by the patient's family Exclusion Criteria: irregular lobulated hematoma (volume of hematoma can not be calculated accurately), such as intraventricular hemorrhage; severe liver disease or impaired liver function; pregnant or lactating women; history of using anticoagulation or antiplatelet aggregation drug (including Cilostazol, aspirin, dipyridamole, heparin, low molecular weight heparin, hirudin, dabigatran, and warfarin); non-accepted informed consent
Facility Information:
Facility Name
Shenzhen second people's hospital
City
Shenzhen
State/Province
Guangdong
ZIP/Postal Code
518000
Country
China
Facility Name
The fifth people's hospital of Longgang District, Shenzhen
City
Shenzhen
State/Province
Guangdong
ZIP/Postal Code
518035
Country
China
Facility Name
Baoan District central hospital of Shenzhen
City
Shenzhen
State/Province
Guangdong
ZIP/Postal Code
518102
Country
China
Facility Name
Shajing hospital of Baoan District ,Shenzhen
City
Shenzhen
State/Province
Guangdong
ZIP/Postal Code
518104
Country
China
Facility Name
The second People's hospital of Longgang District, Shenzhen
City
Shenzhen
State/Province
Guangdong
ZIP/Postal Code
518116
Country
China

12. IPD Sharing Statement

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Vitamin K1 in the Treatment of Spontaneous Intracerebral Hemorrhage

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