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Non-gastric Conduit Reconstruction After Esophagectomy

A Prospective Observational Cohort Study of Patients Undergoing Non-gastric Conduit Reconstruction After Esophagectomy to Assess Surgical Outcomes

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07064655
Enrollment
25
Registered
2025-07-15
Start date
2025-07-15
Completion date
2030-12-30
Last updated
2025-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Cancer, Esophagectomy

Keywords

esophageal cancer, esophagectomy, non-gastric conduit reconstruction

Brief summary

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.

Interventions

None listed

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
anastomotic leakage rateFrom enrollment to 6 months after esophagectomy
rate of conduit necrosisFrom enrollment to 6 months after esophagectomy

Contacts

Primary ContactSeong Yong Park, M.D., Ph.D
syparkcs@gmail.com+821053885715

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026