To Evaluate the Effect of Glibenclamide in Reducing Brain Edema of TBI

Beijing Tiantan Hospital76 enrolled

Overview

Brain edema is one of the main mechanisms of secondary brain injury and one factor in the prognosis of traumatic brain injury . The clinical study of glibenclamide in the treatment of brain edema after traumatic brain injury is designed to evaluate whether glibenclamide treatment can improve the blood NSE and S100β levels of severe traumatic brain injury , so order to explore the efficacy and adverse effects of this drug in the treatment of traumatic brain injury .

Traumatic brain injury has high morbidity,disability and mortality ; worldwide, more than 50 million new cases , mainly low and middle-income countries.The annual incidence of craniocerebral trauma in China is (55 - 64) / 100000 , with 770 - 890 thousand new cases,causing nearly 100000 deaths and hundreds of thousands of disabilities , which is a serious public safety problem .Injury mechanisms after traumatic brain injury include primary and secondary brain injury and have a lack of effective treatment .Brain edema is one of the main mechanisms of secondary brain injury and one factor in the prognosis of traumatic brain injury .In recent years , the Sur1-Trpm4 channel was found to play an important role in the onset of brain edema , with increased expression in traumatic brain injury , ischemic stroke , and ischemic and hypoxic encephalopathy , and the specific inhibitor glibenclamide can reduce brain edema .A clinical study of glibenclamide in the treatment of brain edema after traumatic brain injury to evaluate whether glibenclamide treatment can improve the blood NSE and S100β levels of severe traumatic brain injury , so order to explore the efficacy and adverse effects of this drug in the treatment of traumatic brain injury .

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Traumatic Brain Injury

Interventions

glibenclamideDRUG

Glibenclamide was given orally or by nasal feeding

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Closed craniocerebral trauma; 2. The injury time on admission was less than 10 hours; 3. The GCS score was less than 9, and the GCS score was evaluated without sedation or using muscle relaxants; 4. They were 18-75 years old; 5. Authorized close relatives to sign informed consent. Exclusion Criteria: 1. The damage time is uncertain; 2. Penetrating brain injury; 3. With spinal cord injury; 4. Severe and fatal injuries associated with other parts of the body; 5. Pregnant women or pregnancy test positive; 6. Lactating women had lactation needs during the study period; 7. blood suger is lower than 2.8 mmol / L; 8. Renal insufficiency, history of dialysis treatment, or serum creatinine more than 2.5 mg / dl; 9. The total bilirubin was more than 1.5 times of the upper limit; 10. INR was greater than 1.4; 11. Systolic blood pressure was less than 90 and had no response to fluid resuscitation; 12. Allergic to sulfonylureas; 13. There was a history of admission for brain injury, mental or neurological diseases within 3 years before brain injury; 14. The drug use was restricted due to emergency operation within 8 hours after brain injury; 15. There was a history of taking antiplatelet drugs, oral anticoagulants or heparin or low molecular weight heparin 72 hours before brain injury; 16. There was a history of taking sulfonylureas within 30 days before brain injury; 17. There was a history of participating in other drug trials within 30 days before brain injury; 18\. There was a history of G6PD deficiency; 19. There were clinical conditions that other researchers did not consider to meet the inclusion criteria.

Locations (2)

Beijing Tiantan Hospital Affiliated to Capital Medical University

Beijing, Beijing Municipality, China

RECRUITING

Beijing Tongren Hospital, Capital Medical University

Beijing, China

RECRUITING

Outcomes

Primary Outcomes

Serum NSE and S100 β level

change of the serum NSE and S100 β level concentrations

Time frame: at 1st, 3rd,7th days after recruitment

Secondary Outcomes

Glasgow coma scale(GOS) score

Time frame: at 30 days

Hospital mortality

Time frame: at 30 days

The degree of brain edema

measured by CT

Time frame: at 3rd,7th days after recruitment

The degree of midline displacement of brain CT

Time frame: at 3rd,7th days after recruitment

Intracranial pressure

if have

Time frame: up to 7 days

Central Contacts

qing lin

CONTACT

13811127173 13811127173@163.com

Data from ClinicalTrials.gov

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