A prospective comparative study of the sedation between a combination of propofol and dexmedetomidine hydrochloride and propofol alone in esophageal endoscopic submucosal dissection.
Not Applicable
- Conditions
- Superficial esophageal carcinomas or intraepithelial neoplasias scheduled for ESD.
- Registration Number
- JPRN-UMIN000021487
- Lead Sponsor
- Department of Gastroenterology and Hepatology, Yokohama City University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
Patients classified with an ASA physical status higher than II. Patients with a tracheotomy. Patients with any airway disorder. Patients with a cardiac pacemaker. Patients with gastric tube after esophageal surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method