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The effect of amantadine on the recovery of patients with traumatic brain injury

Phase 3
Conditions
brain injury.
Diffuse traumatic brain injury
S06.2
Registration Number
IRCT20190618043934N18
Lead Sponsor
Birjand University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
51
Inclusion Criteria

Age more than 16 years
GCS=8
Possibility of receiving medicine through NG or OG tube
Obtaining consent from the patient to enter the study after she regains consciousness and recovers(????)

Exclusion Criteria

Pregnancy
Diabetes disease
Dyslipidemia
Cancer
Congenital, ischemic and atherosclerotic heart disease
Kidney failure
Patients with unknown identity
Kidney disease
Use of dopanergic agents by the patient
Contraindications for the use of amantadine

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Glasgow Coma Scale. Timepoint: First and before the intervention, the third day of the intervention and the seventh day of the intervention. Method of measurement: Using the Glasgow coma criteria table and clinical examination by a neurosurgery assistant.
Secondary Outcome Measures
NameTimeMethod
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