Last updated: April 21, 2022
Sponsor: Assiut University
Overall Status: Active - Not Recruiting
Phase
3
Condition
Neurologic Disorders
Treatment
N/AClinical Study ID
NCT05340803
ONSD for TBI patients
Ages 18-45 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Middle age patients ( 18- 45 years old).
- Sever TBI (GCS < 8 and in need for mechanical ventilation).
- Stable hemodynamics
Exclusion
Exclusion Criteria:
- Age: younger than 18 or older than 45 years old.
- Mild and moderate TBI (GCS > 8).
- Shocked and hypoxic patients.
- Contraindications to dexmedetomidine as sever hypotension (mean arterial bloodpressure < 60 mmHg), sever bradycardia (heart rate < 45 beat/min), and AV block in thegroup that will be sedated by midazolam and dexmedetomidine (group B).
- Adverse effects of dexmedetomidine in group B and need to stop it as sever hypotension (mean arterial blood pressure < 60 mmHg) , sever bradycardia (heart rate < 45beat/min), and atrial fibrillation.
- Contraindications to magnesium sulfate as heart block, myocardial damage,hypermagnesemia and renal failure in the group that will be sedated by midazolam andmagnesium sulfate (group C).
- Manifestations of magensium toxicity in group C and need to stop infusion if urineoutput < 80 mL in 4 hours, deep tendon reflexes are absent or serum magnesium level > 3.5 mmol/L .
Study Design
Total Participants: 108
Study Start date:
November 01, 2022
Estimated Completion Date:
December 01, 2025