RECRUITING

Trans-nasal Endoscopy for Bariatric Patients

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

This study plans to learn if the EvoEndo Endoscopy system can be used to evaluate, provide and follow up care for upper gastrointestinal tract diseases in the bariatric population. The smallest current scope available for such a technique is an adult transnasal endoscope with a larger diameter, a pulmonary bronchoscope or Ear Nose and Throat (ENT) laryngoscope. This study is evaluating a newly Food and Drug Administration (FDA) cleared ultra-slim, single-use, endoscope specifically designed for transnasal endoscopy to evaluate its use in adult upper tract gastrointestinal diseases. If such a technique is successful it could improve the safety, cost, and access of endoscopic care for patients in need of an endoscopic evaluation for a bariatric medical condition.

Official Title

Use of Sedation-Free Transnasal Endoscopy to Improve Access and Lower Costs of Endoscopic Evaluations in a Bariatric Medical and Surgical Program

Quick Facts

Study Start:2025-12
Study Completion:2027-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06200961

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 90 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Patient 18 years of age and less than 90 years of age with clinically referred for esophagoscopy, gastroscopy, or esophagogastroduodenoscopy (EGD)
  2. 2. Cared for in metabolic and bariatric clinic
  1. 1. Patient \<18 years of age
  2. 2. Medically contraindicated to perform EGD or TNE
  3. 3. Inability to provide informed consent

Contacts and Locations

Study Contact

Michele B Ryan, MS
CONTACT
617-525-8266
mryan@bwh.harvard.edu

Principal Investigator

Christopher C. Thompson, MD, MSc
PRINCIPAL_INVESTIGATOR
Brigham and Womens Hospital

Study Locations (Sites)

Brigham and Women's Hospital
Boston, Massachusetts, 02115
United States

Collaborators and Investigators

Sponsor: Christopher C. Thompson, MD, MSc

  • Christopher C. Thompson, MD, MSc, PRINCIPAL_INVESTIGATOR, Brigham and Womens Hospital

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 Date2025-12
Study Completion Date2027-06

Study Record Updates

Study Start Date2025-12
Study Completion Date2027-06

Terms related to this study

Keywords Provided by Researchers

  • Transnasal Endoscopy (TNE)
  • Esophagogastroduodenoscopy (EGD)
  • Upper Endoscopy
  • Endoscopy

Additional Relevant MeSH Terms

  • Obesity
  • Obesity, Morbid
  • Obese
  • GI Disorders
  • Gastrointestinal Diseases