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NCT07064655Not yet recruiting

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 · Last updated 15 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
25 (estimated)
First submitted
5 Jul 2025
Start date
15 Jul 2025
Primary completion date
15 Jun 2030
Lead sponsor
Samsung Medical Center
NCT number
NCT07064655

What you commit to

  • Study type: Observational
  • Planned participants: 25
  • From 15 Jul 2025 to the primary completion date, 15 Jun 2030
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • 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

Who the study is looking for

  • 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.

Age in the registry: 20 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.