Skip to main content
Clinical Trials/NCT04930146
NCT04930146
Unknown
Not Applicable

To Evaluate the Functional Recovery Effect of Bloodletting Puncture at Jing-well Points on Acute Brain Injury Patients

Chang Gung Memorial Hospital1 site in 1 country72 target enrollmentJune 8, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Traumatic Brain Injury (TBI)
Sponsor
Chang Gung Memorial Hospital
Enrollment
72
Locations
1
Primary Endpoint
GCS(Glasgow Coma Scale)
Last Updated
4 years ago

Overview

Brief Summary

Traumatic brain injury (Traumatic brain injury, TBI) can be derived from various forms of injury, including blunt trauma, penetrating or acceleration/deceleration force caused by head injury.There are some study data show that acupuncture treatment has a superficial effect on the prognosis of traumatic brain injury and can limit the progression of secondary brain injury, but the effect of early bloodletting at the Jing-points on TBI patients still unknown. In our study, the investigators have proposed a randomized, controlled study design and plan to evaluate the efficacy and safety of Jing-point puncture to improve consciousness and neurological function in patients with TBI. In addition, an objective meridian instrument analysis was added to analyze the energy distribution in the meridian of TBI patients.

Registry
clinicaltrials.gov
Start Date
June 8, 2021
End Date
June 7, 2024
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Chang Gung Memorial Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient with moderate to severe head injury are admitted to the ICU (Intensive Care Unit). patient with stable vital sign and the GCS (Glasgow coma volume) between 5-13 will be included.
  • Patient with normal consciousness and no cognitive or motor function disease before brain injury.
  • Patient aged between 20 to 80 years old and is willing to sign the consent (the agent can sign on behalf of patient).

Exclusion Criteria

  • Patients who are vital sign unstable and with severe complication.
  • Patients combined with other terminal illness such as cancer in terminal stage, liver failure, end stage renal failure and so on.
  • Pregnant patients.
  • Any other conditions deemed unsuitable by the physician in charge.
  • Patients (agent of the patient) who did not sign the consent.

Outcomes

Primary Outcomes

GCS(Glasgow Coma Scale)

Time Frame: 4 weeks

To assess the recovery of consciousness. Lower GCS scores are correlated with higher risk of death.

Barthel index

Time Frame: 4 weeks

To assess the activities of daily life.

Muscle power

Time Frame: 4 weeks

To assess the recovery of muscle power.

mGOS(Modified Glasgow Outcome Score)

Time Frame: 4 weeks

To assess the neurological outcomes, score 1 to 5. the higher the score, the better outcome.

RTS (Revised Trauma Score)

Time Frame: 4 weeks

To assess the physiologic condition of patients. The Revised Trauma Score is made up of a three categories: Glasgow Coma Scale, systolic blood pressure, and respiratory rate. The score range is 0-12. A lower score indicates a higher severity of injury.

Secondary Outcomes

  • Meridian energy assessment(4 weeks)

Study Sites (1)

Loading locations...

Similar Trials