Validation of the Utility of Indocyanine Green for Fluorescence Imaging in Pediatric Gastrointestinal Surgery
Phase 2
Recruiting
- Conditions
- D004933neonatal gastrointestinal perforation, necrotizing enterocolitis, congenital intestinal atresia, esonecrotizing enterocolitis
- Registration Number
- JPRN-jRCT1031230519
- Lead Sponsor
- Takeda Masahiro
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
(1) Patients who require pediatric gastrointestinal surgery at the time of consent (neonatal gastrointestinal perforation, necrotizing enterocolitis, congenital intestinal atresia, esophageal atresia, Hirschsprung's disease, anal fistula, etc.)
(2) Subjects who have received a thorough explanation of their participation in this study, and who have obtained the free and voluntary written consent of the research subject's surrogate after full understanding of the subject's condition.
Exclusion Criteria
(1) Those who could not give their consent to participate in the research
(2) Other persons deemed inappropriate as research subjects by the principal investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The postoperative complications (anastomotic suture failure, anastomotic stenosis, and colostomy problems) will be evaluated and observed as evaluation items in the postoperative follow-up. Observation methods will be the same as those used in general medical care, and the frequency of examination will not be increased as a result of participation in this study.
- Secondary Outcome Measures
Name Time Method