About this trial
This study is to collect and analyze the clinical information of patients who underwent reconstruction using conduits other than the stomach, such as the colon and small intestine, after esophagectomy. Currently, reconstruction after esophagectomy is mainly performed using the stomach, and there is very little information on reconstruction using the colon and small intestine.
Therefore, this study aims to collect information on patients who underwent reconstruction using conduits other than the stomach, analyze the surgical performance, find clinical improvements, and build a foundation for future clinical quality improvement.
Eligibility criteria
Qualifiers
Patients who have voluntarily signed an informed consent form and are willing and able to complete all requirements of the study.
Age 20 years or older.
Patients who are scheduled for esophagectomy and reconstruction with a conduit other than a gastric conduit is planned.
Disqualifiers
Patients who do not consent to participate in this study
The investigator determines that the patient should not participate in the study because the investigator believes that the patient will not be able to comply with the study procedures, requirements, and procedures
Trial design
Treatments tested in this trial
- Not listed