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the Investigation of Therapeutic Effect and Platelet Activity After ILIB for Ischemic Stroke Patient

Primary Purpose

Ischemic Stroke

Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Intravascular laser irradiation of blood
Sponsored by
Tri-Service General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Stroke focused on measuring Ischemic Stroke, intravenous laser irradiation of blood, platele activity

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Aged between 20 to 80 years old
  • Able to speak and understand Mandarin/Taiwanese
  • No cognitive impairment
  • Residual motor function impairment (mRS>1)
  • Mild stroke (NIHSS=1-4) or Moderate stroke(NIHSS=5-15)
  • No psychological disease

Exclusion Criteria:

  • Severe stroke (NIHSS=16-42)
  • History of intracerebral hemorrhage and other major surgery
  • History of malignancy, chronic kidney disease
  • Active infection
  • Chronic hepatitis B or Chronic hepatitis C
  • Unstable angina or acute myocardial infarction within 6 months
  • Severe cognition impairment
  • Pregnancy

Sites / Locations

  • Tri-service general hospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

treatment group

control group

Arm Description

The treatment group receive an intravenous helium-neon laser phototherapy. A vein indwelling needle will be placed in their veins located in the upper elbow, and the laser fiber catheter will be introduced through the indwelling cannula. The laser power is set between 2.5 ~ 3.0Mw, 60 minutes each time, once a day for five consecutive days each week, for 2 weeks (total 10 times in one course)

The steps for the control group are the same as the treatment group, except that the output power is adjusted to zero intensity.

Outcomes

Primary Outcome Measures

National Institutes of Health Stroke Scale (NIHSS)
NIHSS is a measure of the severity of symptoms associated with ischemic stroke and is used as a quantitative measure of neurological deficit post stroke. NIHSS score is composed of 11 items, including consciousness, eye movement, visual fields, muscle power of four limbs, limbs ataxia, sensation, language, dysarthria and extinction. Each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment. Total score are between 0-42. Measure before intravenous laser irradiation, three days, one month, and three months after the therapy.
Modified Rankin Scale (mRS)
The Modified Rankin Scale (mRS) is used to measure the degree of disability or dependence in the daily activities in patients who have had a stroke 0: No symptoms at all No significant disability despite symptoms; able to carry out all usual duties and activities Slight disability; unable to carry out all previous activities, but able to look after own affairs without assistance Moderate disability; requiring some help, but able to walk without assistance Moderately severe disability; unable to walk without assistance and unable to attend to own bodily needs without assistance Severe disability; bedridden, incontinent and requiring constant nursing care and attention Dead Measure before intravenous laser irradiation, three days, one month, and three months after the therapy.
Stroke Impact Scale(SIS)
The Stroke Impact Scale (SIS) is a newly developed comprehensive outcome measure consists of items measuring 8 domains- strength, hand function, activities of daily living (ADL) and instrumental ADL, mobility, communication, emotion, memory and thinking, and participation. It was based on feedback from patients and their caregivers. Measure before intravenous laser irradiation, three days, one month, and three months after the therapy.

Secondary Outcome Measures

Platelet activity
Platelet aggregation test. Measure before intravenous laser irradiation, three days, one month, and three months after the therapy.

Full Information

First Posted
July 9, 2022
Last Updated
April 9, 2023
Sponsor
Tri-Service General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05456750
Brief Title
the Investigation of Therapeutic Effect and Platelet Activity After ILIB for Ischemic Stroke Patient
Official Title
The Investigation of Therapeutic Effect and Platelet Activity After Intravenous Laser Irradiation of Blood for Ischemic Stroke Patient
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 28, 2022 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
July 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tri-Service General Hospital

4. Oversight

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

5. Study Description

Brief Summary
The aim of our study is to therapeutic effect and platelet activity after intravenous laser irradiation of blood for ischemic stroke patient
Detailed Description
Background : This research is designed through randomization, control, and double-blind trial to explore the clinical effectiveness of intravenous laser irradiation of blood for ischemic stroke patient; The research will further explore the changes in platelet activity after treatment. The light accelerates blood and cells circulation in the human body, so that protein molecular structure would promote changes. Pain control is indicated in such treatment, but still lacking evidence of neurological symptoms and functional improvement. Purpose:This research is designed through randomization, control, and double-blind trial to therapeutic effect and platelet activity after intravenous laser irradiation of blood for ischemic stroke patient. Furthermore, to establish a new way of clinical rehabilitation therapy. Method: The investigators plan to recruit 20 patients who are between the ages of 20 to 80 years old. The participants are required to have clear conscious and be able to communicate. The patient with mild to moderate stroke ( NIHSS=1-15), which onset between one month to 2 years will be included. The treatment group will receive an intravenous helium-neon laser phototherapy. A vein indwelling needle will be placed in their veins located in the upper elbow, and the laser fiber catheter will be introduced through the indwelling cannula. The power is set between 2.5 ~ 3.0Mw, 60 minutes each time, once a day for five consecutive days each week, for 2 weeks (total 10 times in one course). The steps for the control group are the same, except that the output power is adjusted to zero intensity. This plan will be explained to the patient in detail during the outpatient visit and patients will sign the consent form upon agreement. Before intravenous laser irradiation, three days, one month, and three months after the therapy, 20 ml of autologous peripheral venous blood need to be drawn for basic blood tests and platelet activity tests. At the same time, the clinical functions of patients will be evaluated, including NIHSS, mRS and Stroke Impact Scale (SIS).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Stroke
Keywords
Ischemic Stroke, intravenous laser irradiation of blood, platele activity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
treatment group
Arm Type
Experimental
Arm Description
The treatment group receive an intravenous helium-neon laser phototherapy. A vein indwelling needle will be placed in their veins located in the upper elbow, and the laser fiber catheter will be introduced through the indwelling cannula. The laser power is set between 2.5 ~ 3.0Mw, 60 minutes each time, once a day for five consecutive days each week, for 2 weeks (total 10 times in one course)
Arm Title
control group
Arm Type
Sham Comparator
Arm Description
The steps for the control group are the same as the treatment group, except that the output power is adjusted to zero intensity.
Intervention Type
Device
Intervention Name(s)
Intravascular laser irradiation of blood
Intervention Description
Low intensity intravenous laser irradiation of blood phototherapy is a method of a 632.8 nm red light penetrate into a vein through fiber and the brightness is 100 fold of the sun. The light accelerates blood and cells circulation in the human body, so that protein molecular structure would promote changes.
Primary Outcome Measure Information:
Title
National Institutes of Health Stroke Scale (NIHSS)
Description
NIHSS is a measure of the severity of symptoms associated with ischemic stroke and is used as a quantitative measure of neurological deficit post stroke. NIHSS score is composed of 11 items, including consciousness, eye movement, visual fields, muscle power of four limbs, limbs ataxia, sensation, language, dysarthria and extinction. Each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment. Total score are between 0-42. Measure before intravenous laser irradiation, three days, one month, and three months after the therapy.
Time Frame
3 month
Title
Modified Rankin Scale (mRS)
Description
The Modified Rankin Scale (mRS) is used to measure the degree of disability or dependence in the daily activities in patients who have had a stroke 0: No symptoms at all No significant disability despite symptoms; able to carry out all usual duties and activities Slight disability; unable to carry out all previous activities, but able to look after own affairs without assistance Moderate disability; requiring some help, but able to walk without assistance Moderately severe disability; unable to walk without assistance and unable to attend to own bodily needs without assistance Severe disability; bedridden, incontinent and requiring constant nursing care and attention Dead Measure before intravenous laser irradiation, three days, one month, and three months after the therapy.
Time Frame
3 month
Title
Stroke Impact Scale(SIS)
Description
The Stroke Impact Scale (SIS) is a newly developed comprehensive outcome measure consists of items measuring 8 domains- strength, hand function, activities of daily living (ADL) and instrumental ADL, mobility, communication, emotion, memory and thinking, and participation. It was based on feedback from patients and their caregivers. Measure before intravenous laser irradiation, three days, one month, and three months after the therapy.
Time Frame
3 month
Secondary Outcome Measure Information:
Title
Platelet activity
Description
Platelet aggregation test. Measure before intravenous laser irradiation, three days, one month, and three months after the therapy.
Time Frame
3 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged between 20 to 80 years old Able to speak and understand Mandarin/Taiwanese No cognitive impairment Residual motor function impairment (mRS>1) Mild stroke (NIHSS=1-4) or Moderate stroke(NIHSS=5-15) No psychological disease Exclusion Criteria: Severe stroke (NIHSS=16-42) History of intracerebral hemorrhage and other major surgery History of malignancy, chronic kidney disease Active infection Chronic hepatitis B or Chronic hepatitis C Unstable angina or acute myocardial infarction within 6 months Severe cognition impairment Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yu Chi Su
Phone
886-972333368
Email
vickysu0110@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Liang chen Chen
Phone
886-2-87923311
Ext
12922
Email
clctsgh@yahoo.com.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Liang-Cheng Chen, MD,MS
Organizational Affiliation
Department of Physical Medicine and Rehabilitation, Tri-Service General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tri-service general hospital
City
Taipei
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yu-Chi Su
Phone
886-972333368
Email
vickysu0110@gmail.com

12. IPD Sharing Statement

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