COMPLETED

Evaluation of Extubation Criteria in Children With Upper Respiratory Infection (URI)

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Conditions

Upper Respiratory Tract InfectionsExtubation criteriaPediatric AnesthesiaOutpatient surgery

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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 investigators are currently completing a data collection to try to optimize pediatric patients' preoperative screening, in the setting of an upper respiratory infection.

Official Title

A Prospective Observational Study Evaluating Extubation Criteria in Children Less Than 8 Years of Age With Upper Respiratory Infection Undergoing Outpatient or Day Hospital Based Surgery

Quick Facts

Study Start:2019-12-04
Study Completion:2025-07-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT04155892

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:Not specified to 7 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * All study participants must be undergoing general anesthesia and surgery with an endotracheal tube
  2. * The URI group will be participants with a score of at least 3 on our pre-operative URI survey, with planned airway instrumentation with an endotracheal tube (ETT) for their surgical procedure who are to be discharged same day or on postoperative day 1.
  3. * The non URI group will be participants undergoing elective procedures with no URI symptom or recent URI. Defined as no URI or "allergy" symptom within the past 6 weeks and a score of 1 or less on the URI survey, with planned airway instrumentation with an ETT for their surgical procedure who are to be discharged same day or on postoperative day 1.
  1. * History of home oxygen use or ventilator dependence,
  2. * Patients undergoing emergent procedures.
  3. * Patients with cyanotic congenital heart disease.
  4. * Patients receiving a surgical procedure where the duration of post procedure
  5. * admission is anticipated to be greater or equal to 2 postoperative days.
  6. * Patients undergoing anesthesia for imaging procedures alone.
  7. * Patients who are extubated deep intentionally.
  8. * Patients intended to be managed with supraglottic airway.
  9. * Patients undergoing total IV anaesthesia (TIVA).

Contacts and Locations

Principal Investigator

Thomas Templeton, MD
PRINCIPAL_INVESTIGATOR
Wake Forest University Health Sciences

Study Locations (Sites)

Wake Forest University Health Sciences
Winston-Salem, North Carolina, 27157
United States

Collaborators and Investigators

Sponsor: Wake Forest University Health Sciences

  • Thomas Templeton, MD, PRINCIPAL_INVESTIGATOR, Wake Forest University Health Sciences

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 Date2019-12-04
Study Completion Date2025-07-03

Study Record Updates

Study Start Date2019-12-04
Study Completion Date2025-07-03

Terms related to this study

Keywords Provided by Researchers

  • Extubation criteria
  • Pediatric Anesthesia
  • Outpatient surgery

Additional Relevant MeSH Terms

  • Upper Respiratory Tract Infections