ACTIVE_NOT_RECRUITING

Gastric Ultrasound for Estimation of the Aspiration Risk 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

The purpose of this research study is to look at the effectiveness of current anesthesia guidelines regarding food and drink prior to surgery in patients who are likely to have food and drink remain in their stomach longer than might ordinarily be expected.

Official Title

Gastric Ultrasound for Estimation of the Aspiration Risk in High Aspiration-risk Surgical Patient Populations

Quick Facts

Study Start:2018-03-27
Study Completion:2026-07-14
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT03310528

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 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Presenting for upper GI endoscopy procedures or surgical repair of a trauma- related injury
  2. * Expected to have an oral-gastric tube placed as part of scheduled procedure
  3. * Willing to undergo an ultrasound exam
  4. * Patients ≥ 18 years of age
  1. * Unwilling to undergo an ultrasound exam
  2. * Oral-gastric tube placement is not indicated
  3. * Oral-gastric tube placement is contraindicated
  4. * Pregnant patients and patients from defined vulnerable populations (ex. pediatric patients, mentally handicapped patients, prisoners, etc.)
  5. * Surgical trauma patients who are not expected to have an OG tube placed during surgery
  6. * Patients with history of gastric bypass surgery
  7. * Patients that are gastrostomy tube dependent

Contacts and Locations

Principal Investigator

Cameron Smith, MD, PhD
PRINCIPAL_INVESTIGATOR
University of Florida

Study Locations (Sites)

United States, Florida UF Health
Gainesville, Florida, 32610-3003
United States

Collaborators and Investigators

Sponsor: University of Florida

  • Cameron Smith, MD, PhD, PRINCIPAL_INVESTIGATOR, University of Florida

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 Date2018-03-27
Study Completion Date2026-07-14

Study Record Updates

Study Start Date2018-03-27
Study Completion Date2026-07-14

Terms related to this study

Keywords Provided by Researchers

  • Aspiration risk
  • GI Endoscopy
  • Fasting guidelines
  • Delayed gastric emptying

Additional Relevant MeSH Terms

  • Respiratory Aspiration of Gastric Contents