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For Patients With Ischemic Stroke, Clinically Study the Effectiveness and Safety of Butylphthalide.

Primary Purpose

Stroke, Cerebral Infarction, Brain Infarction

Status
Recruiting
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Butylphthalide
Sponsored by
Qianfoshan Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Butylphthalide, Ischemic Strokes

Eligibility Criteria

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

Inclusion Criteria:

  • 1. Female or male aged ≥ 18 years.
  • 2. Acute ischemic stroke within 48 hours of onset
  • 3. Examination to exclude intracranial hemorrhage
  • 4. Provision of informed consent.

Exclusion Criteria:

  • 1.Head CT or MRI suggests the presence of intracranial hemorrhagic disease
  • 2.Patients with cerebral embolism or suspected cerebral embolism with severe atrioventricular block disease, atrial fibrillation, myocardial infarction, heart valve disease, infective endocarditis, heart rate less than 50 beats per minute
  • 3.Abnormal liver function (transaminase ALT or AST exceeding the upper limit of normal), abnormal renal function (creatinine exceeding the upper limit of normal), or suffering from other serious systemic diseases, etc
  • 4.Allergy to Butylphthalide

Sites / Locations

  • Shandong Provincial Qianfoshan HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

A group of patients with ischemic stroke were treated with butylphthalide injection and capsules

Arm Description

Patients eligible for inclusion and exclusion are only divided into one group, no controls or other.

Outcomes

Primary Outcome Measures

The incidence of adverse events caused by treatment
In a clinical trial, the probability of an unexpected and adverse medical event that occurs after a patient or clinical subject receives a trial drug, but it does not necessarily have a causal relationship with the treatment.

Secondary Outcome Measures

NIHSS
NIH stroke scale (NIHSS) to assess the degree of neurological deficit in stroke patients. The score ranges from 0 to 42 points, the higher the score, the more severe the nerve damage. Patients with a baseline assessment of> 16 points are likely to die, while those with a score of <6 are likely to recover well; for each additional point, the probability of a good prognosis is reduced by 17%
mRS
Modified Rankin scale (mRS) is an indicator of the efficacy of functional disability. The score ranges from 0 to 5 points, and the clinical score will be increased to 6 points to indicate death. The higher the score, the more disability the patient is.
Correlation between blood drug concentration and adverse events
Try to find the relationship between pharmacokinetic parameters and adverse events

Full Information

First Posted
September 20, 2021
Last Updated
May 6, 2022
Sponsor
Qianfoshan Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05068349
Brief Title
For Patients With Ischemic Stroke, Clinically Study the Effectiveness and Safety of Butylphthalide.
Official Title
A Real-world Study on the Effectiveness and Safety of Butylphthalide in the Treatment of Ischemic Stroke.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 7, 2022 (Actual)
Primary Completion Date
September 2025 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Qianfoshan Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a prospective, open, single-arm, the real world of clinical trials. The researchers plan to recruit 300 eligible patients. The main purpose of this study is to evaluate the effectiveness and safety of butylphthalide in the treatment of ischemic stroke, and to establish a population pharmacokinetic model of butylphthalide in elderly patients to explore its blood drug concentration. Correlation with its efficacy and adverse reactions.
Detailed Description
Ischemic stroke is one of the diseases that seriously threaten human health, with the characteristics of high incidence, high disability and high recurrence rate. Patients will not only suffer from impaired physical function, but also mental symptoms, social function and other obstacles, which seriously affect the quality of life. Butylphthalide can improve the damage of central nervous system in patients with acute ischemic stroke, and can promote the improvement of patients with neurological deficits. Regarding the treatment of ischemic stroke with butylphthalide, there is still a lack of big data research based on real-world efficacy and safety; there is a lack of data on the pharmacokinetics of elderly patients and their correlation with adverse reactions. Thus, it is estimated that 300 patients will be enrolled and given intravenous butylphthalide sodium chloride injection 25mg twice a day for 7-14 days, and then oral butylphthalide soft capsule 0.2g three times a day for 76-83 days. The patients will be collected for experiment before and after treatment. Laboratory data, electrocardiogram, NIHSS, mRS, combined medication and adverse events, etc., to evaluate the effectiveness and safety of butylphthalide in the treatment of ischemic stroke. In addition, a population pharmacokinetic model of butylphthalide in elderly patients was established for 50 of them.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Cerebral Infarction, Brain Infarction, Brain Ischemia, Nervous System Diseases, Central Nervous System Diseases, Vascular Diseases
Keywords
Butylphthalide, Ischemic Strokes

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Model Description
A single-group clinical trial is a study with only one group, and no corresponding control group is designed for the experimental group.
Masking
None (Open Label)
Masking Description
Intervention measures are closer to the real-world clinical environment to make up for the shortcomings of RCT.
Allocation
N/A
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A group of patients with ischemic stroke were treated with butylphthalide injection and capsules
Arm Type
Experimental
Arm Description
Patients eligible for inclusion and exclusion are only divided into one group, no controls or other.
Intervention Type
Drug
Intervention Name(s)
Butylphthalide
Other Intervention Name(s)
3-n-Butylphthalide
Intervention Description
Butylphthalide sodium chloride injection 25mg, 2 times a day, 7-14 days, followed by 0.2g butylphthalide soft capsules, 3 times a day, 76-83 days, a total of 90 days.
Primary Outcome Measure Information:
Title
The incidence of adverse events caused by treatment
Description
In a clinical trial, the probability of an unexpected and adverse medical event that occurs after a patient or clinical subject receives a trial drug, but it does not necessarily have a causal relationship with the treatment.
Time Frame
90 days
Secondary Outcome Measure Information:
Title
NIHSS
Description
NIH stroke scale (NIHSS) to assess the degree of neurological deficit in stroke patients. The score ranges from 0 to 42 points, the higher the score, the more severe the nerve damage. Patients with a baseline assessment of> 16 points are likely to die, while those with a score of <6 are likely to recover well; for each additional point, the probability of a good prognosis is reduced by 17%
Time Frame
90 days
Title
mRS
Description
Modified Rankin scale (mRS) is an indicator of the efficacy of functional disability. The score ranges from 0 to 5 points, and the clinical score will be increased to 6 points to indicate death. The higher the score, the more disability the patient is.
Time Frame
90 days
Title
Correlation between blood drug concentration and adverse events
Description
Try to find the relationship between pharmacokinetic parameters and adverse events
Time Frame
90 days
Other Pre-specified Outcome Measures:
Title
hemoglobin concentration
Description
The normal range of hemoglobin concentration is 120-160g/L for adult males and 110-150g/L for adult females
Time Frame
90days
Title
ECG
Description
The electrocardiogram (ECG) mainly checks whether the patient's heart rate, PR interval, QRS interval, and QT interval are within the normal range.
Time Frame
90days
Title
White blood cell count
Description
White blood cell normal value parameters: adult white blood cell normal value (4.0~10.0)*109 /L
Time Frame
90days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1. Female or male aged ≥ 18 years. 2. Acute ischemic stroke within 48 hours of onset 3. Examination to exclude intracranial hemorrhage 4. Provision of informed consent. Exclusion Criteria: 1.Head CT or MRI suggests the presence of intracranial hemorrhagic disease 2.Patients with cerebral embolism or suspected cerebral embolism with severe atrioventricular block disease, atrial fibrillation, myocardial infarction, heart valve disease, infective endocarditis, heart rate less than 50 beats per minute 3.Abnormal liver function (transaminase ALT or AST exceeding the upper limit of normal), abnormal renal function (creatinine exceeding the upper limit of normal), or suffering from other serious systemic diseases, etc 4.Allergy to Butylphthalide
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xueyan Cui
Phone
15053180972
Email
qfscxy@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Shuxian Lv
Phone
15154126233
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xin Huang
Organizational Affiliation
Qianfoshan Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Shandong Provincial Qianfoshan Hospital
City
Jinan
State/Province
Shandong Provincial
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xin Huang
Email
13791120711@126.com
First Name & Middle Initial & Last Name & Degree
Xueyan Cui
Email
qfscxy@126.com
First Name & Middle Initial & Last Name & Degree
Shuxian Lv

12. IPD Sharing Statement

Plan to Share IPD
Yes

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For Patients With Ischemic Stroke, Clinically Study the Effectiveness and Safety of Butylphthalide.

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