RECRUITING

Organ Retractor Device Study

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 aims to assess the safety and efficacy of an organ retraction device. The study is low risk as it is only being used in patients already undergoing primary robotic bariatric surgery.

Official Title

Boehringer Laboratories Organ Retractor Device Study

Quick Facts

Study Start:2024-03-14
Study Completion:2025-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06754514

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:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * undergoing minimally invasive primary bariatric surgery
  1. * known liver disease

Contacts and Locations

Study Contact

Business Development
CONTACT
4849312338
elagunilla@boehringerlabs.com

Study Locations (Sites)

WakeMed Health & Hospitals
Raleigh, North Carolina, 27610
United States

Collaborators and Investigators

Sponsor: Boehringer Labs LLC

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 Date2024-03-14
Study Completion Date2025-01

Study Record Updates

Study Start Date2024-03-14
Study Completion Date2025-01

Terms related to this study

Additional Relevant MeSH Terms

  • Liver Retraction During Bariatric Surgery