Efficacy of Acupuncture in Patients With Acute Intracranial Hemorrhage


Report Abuse


Investigators propose a research design protocol to evaluate the efficacy of acupuncture in improving function recovery after acute intracranial hemorrhage.

Targeted Conditions

Study Overview

Start Date
March 1, 2024
Completion Date
November 1, 2025
Date Posted
February 6, 2024
Accepts Healthy Volunteers?


Full Address
Chang-Gung Memorial Hospital
Keelung, Taiwan


Minimum Age (years)
Maximum Age (years)
Eligibility Criteria
Inclusion Criteria:

Diagnosis of hemorrhagic stroke by a specialist
Age over 20 years and below 85 years
GCS between 5-13

Exclusion Criteria:

Intracranial hemorrhage resulted from vascular anomalies
Pregnant patients
Intracranial tumor related hemorrhage
Other diseases that can cause neurological deficits, such as old cerebrovascular disease, poliomyelitis, cerebral palsy, spinal cord injury
Organ damage or terminal illness (heart or kidney failure or malignancy)

Study Contact Info

Study Contact Name
Yan Ru Ko
Study Contact Email
Study Contact Phone

Contact Listings Owner Form

Efficacy of Acupuncture in Patients With Acute Intracranial Hemorrhage 0 reviews

Write Your Review

There are no reviews yet.

Write Your Review

Your email address will not be published. Required fields are marked *

Other Details

FDA Regulated Drug?
FDA Regulated Device?
Detailed Description
Stroke is a major cause of death and disability. According to the Ministry of Health and Welfare in Taiwan, stroke accounted for 6.8% of all deaths and was the 4th leading cause of death in Taiwan in 2020. Stroke can be divided into acute, subacute, and chronic stages, and the initial severity of stroke affects recovery from sequelae. Therefore, how to effectively improve the sequelae and accelerate the recovery of patients through early interventions is an important issue. This study aimed to investigate the effect of early acupuncture treatment in the acute stage of hemorrhagic stroke. Subjects will be divided into two main groups by random assignment. The intervention group will be treated with traditional acupuncture, while the control group will be treated with pseudo-acupuncture(superficial acupuncture). The treatment frequency was 3 times a week for at least one week. Consciousness, neurological status and disability status were assessed before treatment, at the end of the first week, the second week and the third week, and biomarker were examined before and after treatment
NCTid (if applicable)