Actively Recruiting

Age: 18Years - 89Years
All Genders
ID05950438

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

Age: 18Years - 89Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Surgery day and hospitalization period

Participants undergo elective robotic transhiatal esophagectomy and receive immediate post-operative care.

1 hospitalization period including surgery

Post-operative Follow-up

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

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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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