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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04930146
Enrollment
72
Registered
2021-06-18
Start date
2021-06-08
Completion date
2024-06-07
Last updated
2021-06-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Traumatic Brain Injury (TBI)

Keywords

Traumatic brain injury, TBI, Bloodletting, acupuncture

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.

Interventions

OTHERacupuncture and bloodletting

bloodletting at the well points of both hands and feet and acupuncture in DU26, DU24 3 times per week for 4 weeks, total 12 treatments.

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. 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. 2. Patient with normal consciousness and no cognitive or motor function disease before brain injury. 3. 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

1. Patients who are vital sign unstable and with severe complication. 2. Patients combined with other terminal illness such as cancer in terminal stage, liver failure, end stage renal failure and so on. 3. Pregnant patients. 4. Any other conditions deemed unsuitable by the physician in charge. 5. Patients (agent of the patient) who did not sign the consent.

Design outcomes

Primary

MeasureTime frameDescription
GCS(Glasgow Coma Scale)4 weeksTo assess the recovery of consciousness. Lower GCS scores are correlated with higher risk of death.
Barthel index4 weeksTo assess the activities of daily life.
Muscle power4 weeksTo assess the recovery of muscle power.
mGOS(Modified Glasgow Outcome Score)4 weeksTo assess the neurological outcomes, score 1 to 5. the higher the score, the better outcome.
RTS (Revised Trauma Score)4 weeksTo 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

MeasureTime frameDescription
Meridian energy assessment4 weeksTo assess meridian energy by Meridian Energy Analysis Device (M.E.A.D. )

Countries

Taiwan

Contacts

Primary Contactwei Ling Chou
wenni1207@cgmh.org.tw+886 975360906

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026