PAravertebral CaTheter Versus Epidural Analgesia in Totally Minimally Invasive Esophagectomies
NCT07434739
Digestive System Diseases, Digestive System Neoplasms
Lille, France
View Trial DetailsNCT Number: NCT07064655
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.
Trial opening soon.
Get Notified20 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: From enrollment to 6 months after esophagectomy
Time frame: From enrollment to 6 months after esophagectomy
Contact information is provided by the study sponsor or research team.
Samsung Medical Center
Other
A Prospective Observational Cohort Study of Patients Undergoing Non-gastric Conduit Reconstruction After Esophagectomy to Assess Surgical Outcomes
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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