Overview
A randomized, double-blind, positive drug/placebo parallel controlled, multicenter, phase III clinical trial of L-oxiracetam injection to improve memory and cognitive Impairment in patients with craniocerebral injury.
Eligibility
Inclusion Criteria:
- Age 18-75 years old (including upper and lower limits), male or female
- Craniocerebral injury meets all of the following conditions: This diagnosis has a clear head trauma, closed head injury, or head injury with cerebrospinal fluid ear leak and / or nasal leak and / or intracranial gas accumulation; MRI or CT confirmed intracranial hemorrhage above the cerebellum (including cerebral contusion, subarachnoid hemorrhage, epidural hematoma, subdural hemorrhage, intracranial hematoma, etc.), with or without transient coma; Craniocerebral injury is classified as mild or moderate (GCS score 10-15 points); Conservative treatment.
- Within 72 hours after head injury, patients with stable and mentally handicapped mental state examination (MMSE) scores are lower than normal.
- The legal representative and / or patient agree to participate in this clinical trial and sign an informed consent form.
Exclusion Criteria:
- People who are known or suspected to be allergic to the test drug and its ingredients.
- After the injury, drugs that improve cognitive function such as the prohibited drugs listed in the protocol have been used.
- With a history of severe traumatic brain injury, a history of cerebrovascular accidents, and structural craniocerebral lesions.
- With diseases such as speech and hearing impairment that cannot cooperate with the completion of cognitive function assessment.
- A secondary brain injury occurred after the craniocerebral injury.
- Those who need craniotomy or extraventricular drainage.
- Combining with other serious large organ damage or serious complications may affect the test Life.
- Patients with active epilepsy who had seizures within 1 year.
- Patients with severe liver and kidney disease.
- Complicated with severe heart disease, lung disease, blood and hematopoietic diseases, gastrointestinal disease, serious or progressive disease.
- Past or present with a malignant tumor
- Combining neurological and mental disorders that make it impossible or unwilling to cooperate.
- Women who are pregnant, breastfeeding or have a recent birth plan.
- Researchers do not consider it appropriate to participate in the clinical trial.
- Those who have participated in other clinical trials and used test drugs 3 months before the trial.