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Minocycline effects in patients with traumatic brain injury

Not Applicable
Conditions
Head injury.
Cerebral contusion, laceration. traumatic intracerebral haemorrhage, Epidural haemorrhage, Extradural haemorrhage (traumatic), Traumatic subdural haemorrhage
S06.3 ,S06
Registration Number
IRCT201602063014N12
Lead Sponsor
Vice chancellor for research, Mazandaran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

The patients who have surgery within 12 hours after admission? glasgow coma scale less than or equal to 12
Exclusion criteria:
Pregnant women and lactating? hypersensitivity to tetracycline and minocycline medicine? history of systemic lupus erythematosus? incidence of pseudomembranous colitis

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
S100B protein. Timepoint: Day 1 (before intervention) , Days 2, 3, 4 (after intervention). Method of measurement: Spectrophotometry kit.;Neuron Specific Enolase (NSE). Timepoint: Day 1 (before intervention), Days 3, 5 (after intervention). Method of measurement: Spectrophotometry kit.
Secondary Outcome Measures
NameTimeMethod
ength of stay in ICU. Timepoint: Hospitalization period in ICU. Method of measurement: Calculating the number of days.;Glasgow coma scale changes. Timepoint: Hospitalization period in ICU. Method of measurement: GCS quiz.
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