A Study to Evaluate the Efficacy and Safety of Local administration of Indocyanine Green in Surgery for Colorectal Neoplasm
- Conditions
- colorectal cancer
- Registration Number
- JPRN-jRCTs031220639
- Lead Sponsor
- Ishihara Soichiro
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 33
(1) With a histological diagnosis of colorectal cancer
(2) Scheduled to have any surgery for the colorectal cancer
(3) With an ECOG performance status of 0 or 1
(4) Aged 18 years and above at the time of informed consent is taken
(5) Male or female
(6) Able and willing to give written informed consent with sufficient understanding after having received sufficient explanation
(1) With allergy to indocyanine green
(2) With iodine allergy or with allergy to iodine contrast
(3) With severe liver failure, renal failure, or cardiac disease
(4) With bowel obstruction
(5) With intraperitoneal infection (e.g. peritonitis or intraperitoneal abscesses)
(6) Difficult colonoscopy
(7) Having a history of severe drug allergy or severe side effects
(8) Pregnant, unwilling to practice contraception during the study, or lactating female
(9) Judged as ineligible by clinical investigators
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method