Randomized, double-blind study to evaluate the sensitivity and painfulness of different concentration of iodine solution during endoscopic examination to detect esophageal squamous epithelial tumor.
Not Applicable
- Conditions
- esophageal squamous epithelial tumor
- Registration Number
- JPRN-UMIN000029796
- Lead Sponsor
- Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Department of Gastroenterology and Hepatology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
1) The patients treated by chemotherapy or radiotherapy and surgery for esophageal SCC or head and neck cancer. 2) A history of iodine hypersensitivity 3) A patient with sedative drugs 4) Pregnant or breast-feeding woman 5) A patient who has not provided written informed consent to participate in this study. 6) In certain circumstances that the researchers determined it was not suitable for the research
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method