The primary goal of this study is to collect short-term and long-term health outcomes of a robotic transhiatal esophagectomy procedure. Clinical (or health) outcomes measure the effect of the procedure on your overall health status. During this procedure, the surgeon will remove all or part of your esophagus. We want to identify patients who will have this procedure. We will look at data elements before, during, and after your procedure to understand the impact of this surgery on your post-operative clinical outcomes.
Age range
18 Years – 89 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of Participants with Anastomotic Leak
Timeframe: During first 3 months postop
Number of Participants with Esophageal Stricture
Timeframe: During first 3 months postop
Number of Participants with Pneumonia
Timeframe: During first 3 months postop
Number of Participants Requiring Ventilation >48 Hours
Timeframe: During first 3 months postop
Number of Participants with Empyema
Timeframe: During first 3 months postop
Number of Participants with Pulmonary Embolism
Timeframe: During first 3 months postop
Number of Participants with Deep Venous Thrombosis
Timeframe: During first 3 months postop
Number of Participants with Gastric Outlet Obstruction
Timeframe: During first 3 months postop
Number of Participants with Stroke
Timeframe: During first 3 months postop
Number of Participants with Atrial Fibrillation
Timeframe: During first 3 months postop
Number of Participants with Vocal Cord Paralysis
Timeframe: During first 3 months postop
Number of Participants with Myocardial Infarction
Timeframe: During first 3 months postop
Number of Participants with Chylothorax
Timeframe: During first 3 months postop
Number of Participants with Acute Renal Injury
Timeframe: During first 3 months postop
Number of Participants with Wound Infections
Timeframe: During first 3 months postop
Rates of Re-operation
Timeframe: During first 3 months postop
Rates of Re-Admission
Timeframe: During first 3 months postop
Number of Participants with Intensive Care Unit (ICU) Stay
Timeframe: During first 3 months postop
Rates of Length of Hospital Stay
Timeframe: Postoperative
Rates of 30-day Survival
Timeframe: Postoperative
Rates of 90-day Survival Rates
Timeframe: Postoperative