International Trial of Efficacy of Cytoflavin in Head Trauma

Inclusion Criteria:

1. Age from 18-60 (inclusive).

2. Clinical diagnosis of TBI, cerebral contusion of moderate severity withoutcompression.

3. The written consent of the legal representative or the decision of the council toinclude the patient in the study.

4. Possibility of a full assessment of eye opening, speech and motor response by GCS.

5. GCS at the time of inclusion 9 - 14 (inclusive).

6. Time of initiation of study drug therapy within 24 hours after the estimated ordetermined time of injury.

7. The presence of post-traumatic amnesia, confusion and disorientation.

8. Absence of indications for neurosurgery or other surgical intervention under generalanesthesia.

9. Normal brain CT scan, or the presence of subarachnoid hemorrhage and / or contusionfoci of I-III types according to Kornienko and / or limited or diffuse cerebraledema.

10. The expected duration of hospital stay >= 10 days.

11. Absence of a disabling neurological or mental illness, information about thepatient's disability prior to injury.

12. Possibility to perform all procedures stipulated by the study protocol

Exclusion Criteria:

1. The need to use the therapy prohibited by the study protocol.

2. Concomitant injury, except for cases of damage to the skeleton, soft tissues,internal organs, which do not require (1) surgical intervention under generalanesthesia, and (2) are not an independent indication for hospital treatment.

3. Past / planned surgical intervention for the current episode of trauma under generalanesthesia.

4. Penetrating open TBI.

5. Presence of the following lesions on the results of computed tomography (CT) of thebrain performed prior to the patient's randomization:

6. epidural hematoma or subdural hematoma;

7. evidence of a previous head injury based on CT results;

8. type IV contusion foci according to Kornienko's classification.

9. Presence of any of the following risk factors for secondary brain injury at any timeafter TBI: hypoxia (SpO2 <90% based on pulse oximetry results); hypotension (systolic blood pressure <90 mm Hg) or shock;hypothermia (body temperature <35 ° C);clinical signs of respiratory failure, the need for mechanical ventilation.

10. Drug addiction.

11. Alcohol in saliva >=2 ‰ or a previous diagnosis of alcohol dependence.

12. Depression of consciousness, presumably resulting from other reasons (for example,alcohol, drugs, drugs, poisonous substances).

13. The presence of aphasia due to focal brain damage, which prevents communication withthe researcher.

14. Status epilepticus at the time of admission to the hospital or condition after anepileptic seizure.

15. Pregnant and lactating women.

16. Availability of information about concomitant chronic disease in the stage ofdecompensation.

17. Intolerance to the components of CYTOFLAVIN®, anamnestic data on drug allergy tosuccinic acid, riboflavin, inosine, or nicotinamide.

18. Severe renal or heart failure requiring restriction of the volume of injected fluid.

19. The presence of a condition or disease that, in the opinion of the investigator,jeopardizes the patient's safety if the patient participates in the study, or mayinterfere with the performance of examination procedures, an objective assessment ofthe patient's condition, or distort the assessment of the outcome of TBI.

20. Participation in any clinical study less than 3 months before the start of thestudy.

21. Patients who are employees of the research center and their families.

22. Language barrier.

23. Availability of information that the patient is a stateless person or a citizen ofanother state