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An fNIRS Study of Motor Cortical Activation in Stoke Patients

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Capital Medical University

Status

Enrolling

Conditions

Acute Ischemic Stroke

Study type

Observational

Funder types

Other

Identifiers

NCT05376098
haojunwei7

Details and patient eligibility

About

The investigators evaluate the activation and connectivity of patients' motor regions in the acute phase of ischemic stroke by fNIRS.

Full description

This study aims to analyze the progress of brain recovery from upper-limb deficit due to acute ischemic stroke, using Functional Near-infrared Spectroscopy(fNIRS) as the main neural imaging method. Fifty patients having experienced a stroke onset within seven days will be recruited from the emergency room. The fNIRS signals will be recorded bilaterally over the contralateral sensorimotor cortex, the premotor area, the supplementary motor area, the primary motor cortex for 14 days after being diagnosed. Then compute activation and connectivity of the regions. The motor function data measured by the assessment scales, as well as the behavioral record during the fNIRS motor tasks will be collected as well.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The diagnosis of ischemic stroke should meet the diagnostic criteria of the "China Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2018".
  • 18 years old≤ age ≤ 75 years old.
  • Cerebral ischemic stroke onset within 7 days.
  • First onset.
  • Upper limb motor dysfunction.

Exclusion criteria

  • Unstable vital signs.
  • Complicated with other diseases in the nervous system.
  • Combined with other serious disease states: circulatory system, respiratory system,
  • motor system diseases, such as atrial fibrillation, heart failure, lung infection, severe liver and kidney dysfunction, lower limb venous thrombosis, etc.
  • Upper limb dysfunction caused by other reasons, such as fractures, upper limb deformities, etc.
  • Contraindicated to imaging tests, such as metal implantation, claustrophobia, and severe obesity.
  • Those who cannot complete the examination due to other reasons, such as mental disorders, cognitive dysfunction, etc.
  • Other causes: alcoholism; pregnancy; skull defects; soft tissue injuries at the site of examination; visual impairment, etc.

Trial contacts and locations

1

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Central trial contact

haijie Liu; Junwei Hao

Data sourced from clinicaltrials.gov

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