Comparing the effectiveness of propofol-remifentanil with propofol-dexmedetomidine in reducing pain after awake craniotomy surgery
Phase 3
Recruiting
- Conditions
- Awake craniotomy.Other disorders of brain in diseases classified elsewhere
- Registration Number
- IRCT20151221025641N5
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 64
Inclusion Criteria
The patient should be a candidate for craniotomy surgery using the sleep-awake-asleep method;
The patient does not have a previous craniotomy history;
The patient does not have a contraindication for full anesthesia;
The patient's age is between 20 and 50 years;
The patient does not have a history of allergy to any of the drugs under study.
Exclusion Criteria
In addition to craniotomy, the patient needs to perform another surgery at the same time;
Pregnancy;
Breast feeding;
The patient has simultaneously heart, renal or liver failure;
Severe obesity (BMI>30 kg/m2);
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method