Collecting health outcomes from robotic esophagectomy procedures
A Prospective Clinical Registry Investigating Outcomes of Elective Robotic Transhiatal Esophagectomy
This study is collecting health information from patients who have robotic esophagectomy surgery to see how it affects their recovery and overall health.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 25 (estimated) |
| Ages | 18 Years to 89 Years |
| Sex | All |
| Sponsor | Northwestern University Academic / other |
| Locations | 1 site (Chicago, Illinois) |
| Trial ID | NCT05950438 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather both short-term and long-term health outcomes from patients undergoing elective robotic transhiatal esophagectomy. The research will involve collecting clinical and demographic data before, during, and after the surgical procedure to assess its impact on overall health status. By focusing on this minimally invasive surgical approach, the study seeks to identify factors that contribute to improved patient outcomes and inform future surgical practices. The study is being conducted at Northwestern Memorial Hospital, which specializes in this type of surgery.
Who should consider this trial
Good fit: Ideal candidates include adult patients aged 18 and older who are undergoing elective esophagectomy for any indication.
Not a fit: Patients undergoing emergent esophagectomy or those unable to provide consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of the benefits and risks associated with robotic transhiatal esophagectomy, leading to improved patient outcomes.
How similar studies have performed: Other studies have shown success with minimally invasive surgical approaches, suggesting potential for positive outcomes in this area.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients (18 years or older) * Patients undergoing elective esophagectomy for any indication * Patients who have already had an elective esophagectomy for any indication * Patients with consent providing capacity Exclusion Criteria: * Patients undergoing emergent esophagectomy * Adults unable to consent * Individuals who are not yet adults (infants, children, teenagers) * Pregnant women * Prisoners * Vulnerable Populations
Where this trial is running
Chicago, Illinois
- Northwestern University — Chicago, Illinois, United States (Recruiting)
Study contacts
- Principal investigator: Ankit Bharat, MD — Northwestern University
- Study coordinator: Ankit Bharat, MD
- Email: ankit.bharat@northwestern.edu
- Phone: 312-926-7628
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.