Clinical trial · Observational
Non-gastric Conduit Reconstruction After Esophagectomy
A Prospective Observational Cohort Study of Patients Undergoing Non-gastric Conduit Reconstruction After Esophagectomy to Assess Surgical Outcomes
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Esophageal Cancer | Malignant Esophageal Neoplasm | CURATED_EXACT | 0.92 |
| Esophagectomy | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (1)
- label
- Non-gastric conduit group
- description
- Patients who received the reconstruction other than a gastric conduit after esophagectomy
Primary outcomes (2)
- measure
- anastomotic leakage rate
- timeFrame
- From enrollment to 6 months after esophagectomy
- measure
- rate of conduit necrosis
- timeFrame
- From enrollment to 6 months after esophagectomy
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
Show eligibility criteria text
Inclusion Criteria: * 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. Exclusion Criteria: * 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
References
Publications (0)
Data not yet available