Status:

UNKNOWN

Acute Ischemic Apoplexy Syndrome Specificity and Acupuncture Intervention Research

Lead Sponsor:

Shanghai University of Traditional Chinese Medicine

Conditions:

Acute Ischemia

Eligibility:

All Genders

45-80 years

Phase:

NA

Brief Summary

This project optimizes the TCM Symptoms and Symptoms Scale. A curative effect evaluation system of acupuncture in the treatment of acute ischemic stroke is formed to provide clinical evidence by the f...

Detailed Description

Based on the previous work, this project optimizes the TCM Symptoms and Symptoms Scale. Through the cohort study method, 194 patients with acute ischemic stroke were evaluated for neurological impairm...

Eligibility Criteria

Inclusion

  • (1) It meets the diagnostic criteria in the "Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2014"; with the support of brain CT or MRI imaging examination, the vital signs are stable, the state of consciousness is clear, and the GCS\>8 points; (2).Onset is less than 2 weeks; (3). There is no indication for thrombolysis, or the patient do not accept thrombolysis; (4). For moderate to severe patients, the National Institute of Health Stroke Scale (NIHSS) ≥ 4 points;(5).Glasgow coma standard (GCS)\>7 points;(6).No serious disability before admission, and modified Rankin Scale (mRS) ≤ 3;(7). The patient himself or his immediate family members signed the informed consent form.

Exclusion

  • \- (1) Cerebral hemorrhage or subarachnoid hemorrhage; (2) Cerebellar and brainstem infarction (including lacunar infarction); (3) Cerebral herniation is formed upon admission; (4) Patients with severe heart, lung, liver, and kidney diseases; (5) Severe upper gastrointestinal bleeding occurred after the onset; (6) The patient has participated in other clinical trials within the past 3 months; (7) Patients with mental illness, or those with severe cognitive impairment (MMSE score ≤9 points) (8) Those with a pacemaker, a metal foreign body at the treatment site, or a severe bleeding tendency.
  • (9) The investigator believes that other diseases accompanied by the patient may interfere with the correct evaluation of neurological function, or participating in this trial may cause other complications in the patient.

Key Trial Info

Start Date :

October 1 2020

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 1 2022

Estimated Enrollment :

194 Patients enrolled

Trial Details

Trial ID

NCT04528472

Start Date

October 1 2020

End Date

October 1 2022

Last Update

August 27 2020

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