Investigation and comparison of intravenous infusion of sodium pentotal on the neurological outcomes of patients undergoing decompressive craniectomy
Phase 3
- Conditions
- Craniocerebral Trauma.Traumatic cerebral edema with loss of consciousness of any duration with death due to brain injury prior to regaining consciousness, initial encounterS06.1X7A
- Registration Number
- IRCT20200817048436N1
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Patients with increased ICP that undergo decompressive craniotomy
Exclusion Criteria
Age less than 12 years and over 65 years
Dissatisfaction of the patient or his guardian to participate in the study
Patients with a known psychiatric history
Patients with degenerative underlying brain disease
No swelling of the brain during surgery
Pregnant mothers
Patients with Glasgow Coma Scale/Score: 3 at baseline
Patients with Glasgow Coma Scale/Score: 4 and bilateral pupillary mydriasis at baseline
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Glascow Coma Scale. Timepoint: From the moment of starting treatment until the time of hospitalization and also during 1 and 3 months after that. Method of measurement: Scoring between 3 and 15.;Glasgow Outcome Scale. Timepoint: From the moment of starting treatment until the time of hospitalization and also during 1 and 3 months after that. Method of measurement: Clinical examination of the patient.
- Secondary Outcome Measures
Name Time Method