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The effect of zolpidem and amantadine on the level of consciousness in patients diffuse axonal injury

Phase 3
Conditions
diffuse axonal injury.
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G35-G37
Registration Number
IRCT20191026045243N1
Lead Sponsor
Sari University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
66
Inclusion Criteria

1. Confirmation of axonal injury published by a specialist in neurosurgery
2. GCS less than or equal to 8
3. Age between 15 and 70 years
4. Hospitalized less than 8 hours after injury
5. Informed consent from the patient's companions for inclusion in the study

Exclusion Criteria

1. Patient's or guardian's dissatisfaction with the study
2. A history of drug allergy to zolpidem or amantadine
3. History of any previous brain trauma
4. History of any previous brain procedure

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Increased awareness and speed of recovery for patients with cognitive problems and brain injuries. Timepoint: During these 8 days and up to 3 days after discontinuation of the drug. Method of measurement: Glasgow Coma Scale.
Secondary Outcome Measures
NameTimeMethod
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