RECRUITING

PUSH-IT Continuing Enteral Feeds for Tracheostomy

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 goal of this clinical trial is to evaluate nutrition administration in the time around the tracheostomy in patients with breathing tubes. The main questions it aims to answer are: * Will continuing nutrition up to the time of surgery (tracheostomy) decrease nutrition interruptions, thereby increasing food intake? * Does continuing nutrition up to the time of surgery increase instances of food going into the lungs or lung infections? Researchers will compare patients who have nutrition withheld 6 hours prior to surgery versus those who receive nutrition up until the time of surgery to see if there are differences in food intake, instances of food entering the lungs or lung infections.

Official Title

Prevent Unnecessary Surgeon Holds of Ingestions for Tracheostomy (PUSH-IT)

Quick Facts

Study Start:2023-02-06
Study Completion:2026-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05906472

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. * 18 years or older
  2. * admitted to the intensive care unit (ICU)
  3. * intubated and require tracheostomy
  1. * under 18 years
  2. * unable to obtain informed consent
  3. * deemed clinically brain dead within 7 days of enrollment
  4. * transitioned to comfort measures within 7 days of enrollment
  5. * Pregnant patients
  6. * Prisoners

Contacts and Locations

Study Contact

Eden Nohra, MD
CONTACT
3144439727
edennohra@gmail.com

Principal Investigator

Marcy Jordan, PhD
STUDY_DIRECTOR
University at Buffalo

Study Locations (Sites)

St. Mary's Medical Center
West Palm Beach, Florida, 33407
United States
HCA Research Medical Center
Kansas City, Missouri, 64132
United States
Erie County Medical Center (University at Buffalo)
Buffalo, New York, 14215
United States
Lehigh Valley Health Network
Allentown, Pennsylvania, 18103
United States
University of South Carolina Sch of Medicine /Prisma Health Richland
Columbia, South Carolina, 29203
United States

Collaborators and Investigators

Sponsor: State University of New York at Buffalo

  • Marcy Jordan, PhD, STUDY_DIRECTOR, University at Buffalo

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 Date2023-02-06
Study Completion Date2026-12-31

Study Record Updates

Study Start Date2023-02-06
Study Completion Date2026-12-31

Terms related to this study

Keywords Provided by Researchers

  • tube feed
  • nil per os
  • aspiration
  • pneumonia
  • nutritional delivery

Additional Relevant MeSH Terms

  • Tracheostomy Complication
  • Critical Illness
  • Nutritional Deficiency