RECRUITING

Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair

Conditions

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 aim of this study is to find out if using a certain kind of mesh can reduce the chances of hiatal hernias coming back after anti-reflux surgery. Participants undergoing antireflux surgery will be assigned to one of two groups, a group that has surgery with mesh, or a group that has surgery without mesh.

Official Title

The Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair in Robotic Anti-Reflux Surgery: A Multi-Institutional Randomized Trial

Quick Facts

Study Start:2024-06-10
Study Completion:2030-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06444347

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Documented diagnosis of gastroesophageal reflux disease
  2. * Adults aged 18 years or older
  3. * English speaking
  4. * Subject is planned to undergo surgery for reflux disease
  1. * Physician deems the subject is unable to complete the study due to documented dementia.
  2. * Subject is undergoing emergent surgery.
  3. * Pregnancy
  4. * Patient has known allergy to tetracycline hydrochloride or kanamycin sulfate

Contacts and Locations

Study Contact

Annabel Endean, NP
CONTACT
646-962-5250
ant2028@med.cornell.edu
Niloufar Salehi, MD
CONTACT
nis4017@med.cornell.edu

Principal Investigator

Rasa Zarnegar, MD
PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University

Study Locations (Sites)

University of Southern California Keck School of Medicine
Los Angeles, California, 90033
United States
Louisiana State University School of Medicine
New Orleans, Louisiana, 70112
United States
Washington University School of Medicine
Saint Louis, Missouri, 63110
United States
NYU Langone Health
New York, New York, 10016
United States
Weill Cornell Medicine
New York, New York, 10065
United States
Lenox Hill Hospital
New York, New York, 10075
United States

Collaborators and Investigators

Sponsor: Weill Medical College of Cornell University

  • Rasa Zarnegar, MD, PRINCIPAL_INVESTIGATOR, Weill Medical College of Cornell 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 Date2024-06-10
Study Completion Date2030-07

Study Record Updates

Study Start Date2024-06-10
Study Completion Date2030-07

Terms related to this study

Additional Relevant MeSH Terms

  • Hiatal Hernia