Actively Recruiting
A Prospective Clinical Registry Investigating Outcomes of Elective Robotic Transhiatal Esophagectomy
Led by Northwestern University · Updated on 2026-05-26
120
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to collect and analyze short-term and long-term health outcomes from patients undergoing elective robotic transhiatal esophagectomy, a surgical procedure to remove all or part of the esophagus. The study focuses on adult patients having this procedure to better understand its effects on overall health and post-operative recovery. The registry seeks to identify factors that contribute to improved clinical outcomes and guide future surgical practices. The procedure studied is an elective robotic transhiatal esophagectomy, which involves removing the esophagus and reconstructing it using other parts of the gastrointestinal tract. This minimally invasive surgery is preferred due to generally lower morbidity compared to open surgeries. The study collects clinical and demographic data before, during, and after the procedure to assess various outcomes and surgical details. Participants will provide data on their health status before and after surgery, with researchers monitoring for complications such as leaks, strictures, pneumonia, and other post-operative events during the first three months after surgery. The study includes assessments of operative time, blood loss, and the surgical specimen. Safety and recovery outcomes, including hospital stay length and survival rates at 30 and 90 days post-operation, are also tracked. Participation involves data collection over the short and long term to evaluate the impact of this surgical approach.
CONDITIONS
Brief Title
Investigating Outcomes of Elective Robotic Transhiatal Esophagectomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients (18 years or older)
- Patients undergoing elective esophagectomy for any reason
- Patients who have already had an elective esophagectomy
- Patients able to provide informed consent
You will not qualify if you...
- Patients undergoing emergency esophagectomy
- Adults unable to provide consent
- Individuals under 18 years old
- Pregnant women
- Prisoners
- Vulnerable populations
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Surgery day and hospitalization period
Participants undergo elective robotic transhiatal esophagectomy and receive immediate post-operative care.
1 hospitalization period including surgery
Duration - 3 months
Participants are monitored for complications and recovery during the first 3 months after surgery.
Approximately 6 post-operative visits
Trial Site Locations
Total: 1 location
1
Northwestern University
Chicago, Illinois, United States, 60611
Actively Recruiting
Research Team
A
Ankit Bharat, MD
S
Sara Krezalek, BSN
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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