Fenofol and ketofol conscious sedation for surgical procedures: a randomized double-blind controlled study
Phase 3
Not yet recruiting
- Conditions
- Anaesthesia
- Registration Number
- PACTR202407472796548
- Lead Sponsor
- faculty of medicine . menofia university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Male
- Target Recruitment
- 30
Inclusion Criteria
20 and 60 years
physical status I and II
scheduled for surgical procedures under conscious sedation
Exclusion Criteria
with uncontrolled systemic disease,
allergy to local anaesthetic or study drugs,
chronic analgesic or sedative usage and alcohol or substance abuse
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie fenofol and ketofol's sedative effects in conscious anesthesia?
How does fenofol compare to ketofol in efficacy and safety for surgical sedation in phase III trials?
Are there specific biomarkers that predict patient response to fenofol or ketofol sedation regimens?
What are the potential adverse events associated with fenofol and ketofol in clinical sedation settings?
What are the current drug classes and compounds competing with fenofol and ketofol for conscious sedation?