RECRUITING

Investigating Outcomes of Elective Robotic Transhiatal Esophagectomy

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

A Prospective Clinical Registry Investigating Outcomes of Elective Robotic Transhiatal Esophagectomy

Quick Facts

Study Start:2023-07-11
Study Completion:2028-05-25
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05950438

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 89 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adult patients (18 years or older)
  2. * Patients undergoing elective esophagectomy for any indication
  3. * Patients who have already had an elective esophagectomy for any indication
  4. * Patients with consent providing capacity
  1. * Patients undergoing emergent esophagectomy
  2. * Adults unable to consent
  3. * Individuals who are not yet adults (infants, children, teenagers)
  4. * Pregnant women
  5. * Prisoners
  6. * Vulnerable Populations

Contacts and Locations

Study Contact

Ankit Bharat, MD
CONTACT
312-926-7628
ankit.bharat@northwestern.edu
Sara Krezalek, BSN
CONTACT
312-926-7577
sara.krezalek@nm.org

Principal Investigator

Ankit Bharat, MD
PRINCIPAL_INVESTIGATOR
Northwestern University

Study Locations (Sites)

Northwestern University
Chicago, Illinois, 60611
United States

Collaborators and Investigators

Sponsor: Northwestern University

  • Ankit Bharat, MD, PRINCIPAL_INVESTIGATOR, Northwestern University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-07-11
Study Completion Date2028-05-25

Study Record Updates

Study Start Date2023-07-11
Study Completion Date2028-05-25

Terms related to this study

Keywords Provided by Researchers

  • Robotic Transhiatal

Additional Relevant MeSH Terms

  • Esophagectomy