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

T

Tri-Service General Hospital

Status

Enrolling

Conditions

Ischemic Stroke

Treatments

Device: Intravascular laser irradiation of blood

Study type

Interventional

Funder types

Other

Identifiers

NCT05456750
TSGH-D-111106

Details and patient eligibility

About

The aim of our study is to therapeutic effect and platelet activity after intravenous laser irradiation of blood for ischemic stroke patient

Full 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).

Enrollment

20 estimated patients

Sex

All

Ages

20 to 80 years old

Volunteers

No 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

20 participants in 2 patient groups

treatment group
Experimental group
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)
Treatment:
Device: Intravascular laser irradiation of blood
control group
Sham Comparator group
Description:
The steps for the control group are the same as the treatment group, except that the output power is adjusted to zero intensity.
Treatment:
Device: Intravascular laser irradiation of blood

Trial contacts and locations

1

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Central trial contact

Yu Chi Su; Liang chen Chen

Data sourced from clinicaltrials.gov

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