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Treating Respiratory Emergencies in Children Study (T-RECS)

Primary Purpose

Asthma in Children

Status
Not yet recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Ipratropium Bromide
Sponsored by
Oregon Health and Science University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma in Children

Eligibility Criteria

2 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Ages 2-17 years; AND Transported by EMS through 911 activation; AND Prior history of wheeze/asthma, current asthma symptoms (dyspnea or wheeze); AND At least 4 of the following: Visible use of accessory muscles/retractions Inspiratory and expiratory wheezing or silent chest Abnormal respiratory rate for age For < 6 years ≥ 46 breaths/min For ≥ 6 years ≥ 36 breaths/min Agitation, drowsiness, or confusion Oxygen saturation < 93% on room air Exclusion Criteria: History of albuterol, ipratropium, or dexamethasone allergy Known or suspected pregnancy Prisoner Croup Suspected airway foreign body Respiratory distress not due to bronchospasm/wheeze Parent, legally authorized representative (LAR), subject, and/or family member objects to participation prior to treatment

Sites / Locations

  • University at Buffalo
  • Mecklenburg County EMS
  • University of Utah

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Continue current care

Treatment bundle and checklist

Arm Description

In this arm, participants will be treated using the existing EMS protocol, and evaluate patient outcomes.

In this arm, we will implement a new treatment protocol with the study bundle, and evaluate patient outcomes.

Outcomes

Primary Outcome Measures

Proportion of patients admitted to the hospital in each group
Whether or not the patient was admitted to the hospital after the index EMS encounter

Secondary Outcome Measures

NIH Patient-Reported Outcomes Measurement Information Systems (PROMIS) asthma impact scale
Quality of life score for asthma. Range 0-100. A higher score equates to poorer quality of life.

Full Information

First Posted
August 10, 2023
Last Updated
October 5, 2023
Sponsor
Oregon Health and Science University
Collaborators
University of Utah, University at Buffalo, Wake Forest University Health Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT06074185
Brief Title
Treating Respiratory Emergencies in Children Study
Acronym
T-RECS
Official Title
Treating Respiratory Emergencies in Children Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 1, 2024 (Anticipated)
Primary Completion Date
August 31, 2024 (Anticipated)
Study Completion Date
September 7, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Oregon Health and Science University
Collaborators
University of Utah, University at Buffalo, Wake Forest University Health Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Over 200,000 children have a 911 Emergency Medical Services (EMS) activation for respiratory distress each year, most of whom have acute wheezing. Early treatment in the prehospital setting could more rapidly relieve respiratory distress symptoms, prevent hypoxia, reduce invasive interventions, and reduce the need to be hospitalized, thereby facilitating earlier return to normal daily activities. Preliminary data from one site found hospital admission was reduced from 30% to 21% among children when an EMS system introduced a pediatric asthma protocol with oral dexamethasone. The current standard for Emergency Department (ED) treatment for acute wheezing for children two and older includes inhaled ipratropium and dexamethasone. These treatments have a longstanding history of safety and are effective in preventing hospitalization when used early in the ED. Specific treatment protocols generally direct prehospital care. Ipratropium and dexamethasone are recommended by national EMS organizations that develop model protocols for prehospital care. However, only 25% of EMS agencies from large US metropolitan areas allow ipratropium, and only 10% include dexamethasone in their treatment protocols. A clinical trial is critically needed to evaluate whether the significant EMS resources required to implement interventions for children with life-threatening wheezing that have proven benefit in the ED result in improved patient outcomes. The overall objective of this three-site pilot trial is to address specific questions related to the implementation of the study and ensure its feasibility. The study will be conducted in the Pediatric Emergency Care Applied Research Network (PECARN) EMS Affiliates (EMSAs). The investigators will include patients aged 2-17 who have a 911 call for acute life-threatening wheezing. The specific aims are 1) to develop and produce a prehospital checklist for the treatment bundle, including ipratropium and dexamethasone, 2) to determine the feasibility of collecting patient outcomes for wheezing children treated in the EMS system, and 3) to evaluate the implementation of the EMS treatment bundle and checklist using the Reach, Effectiveness, Adoption, Implementation, and Maintenance (RE-AIM) framework. Our overall hypothesis is that the study will be feasible to implement. This study will provide the necessary data to ensure the eventual trial is feasible, primarily by establishing the ability to measure the outcomes of interest as well as evaluating implementation. This study is innovative by focusing on pediatric care in the prehospital environment, a critical component of our emergency care system that is often neglected in research.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma in Children

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
This is a before-and-after study
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Continue current care
Arm Type
No Intervention
Arm Description
In this arm, participants will be treated using the existing EMS protocol, and evaluate patient outcomes.
Arm Title
Treatment bundle and checklist
Arm Type
Experimental
Arm Description
In this arm, we will implement a new treatment protocol with the study bundle, and evaluate patient outcomes.
Intervention Type
Drug
Intervention Name(s)
Ipratropium Bromide
Other Intervention Name(s)
dexamethasone
Intervention Description
The study intervention involves implementing a treatment bundle that includes inhaled ipratropium bromide and dexamethasone.
Primary Outcome Measure Information:
Title
Proportion of patients admitted to the hospital in each group
Description
Whether or not the patient was admitted to the hospital after the index EMS encounter
Time Frame
Within 24 hours of the index EMS encounter
Secondary Outcome Measure Information:
Title
NIH Patient-Reported Outcomes Measurement Information Systems (PROMIS) asthma impact scale
Description
Quality of life score for asthma. Range 0-100. A higher score equates to poorer quality of life.
Time Frame
6-8 days after the index EMS encounter
Other Pre-specified Outcome Measures:
Title
Rate of successful primary and secondary outcome measurement among participants
Description
We will evaluate the feasibility of collecting the main study outcomes among study participants
Time Frame
Through 8 days after enrollment
Title
Proportion of patients who require a critical care intervention
Description
Use of bag mask ventilation, non-invasive positive pressure ventilation, endotracheal intubation, high-flow nasal cannula, Extra Corporeal Membrane Oxygenation (ECMO), and Cardio Pulmonary Resuscitation (CPR)
Time Frame
Within one week of the index EMS encounter

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ages 2-17 years; AND Transported by EMS through 911 activation; AND Prior history of wheeze/asthma, current asthma symptoms (dyspnea or wheeze); AND At least 4 of the following: Visible use of accessory muscles/retractions Inspiratory and expiratory wheezing or silent chest Abnormal respiratory rate for age For < 6 years ≥ 46 breaths/min For ≥ 6 years ≥ 36 breaths/min Agitation, drowsiness, or confusion Oxygen saturation < 93% on room air Exclusion Criteria: History of albuterol, ipratropium, or dexamethasone allergy Known or suspected pregnancy Prisoner Croup Suspected airway foreign body Respiratory distress not due to bronchospasm/wheeze Parent, legally authorized representative (LAR), subject, and/or family member objects to participation prior to treatment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Matthew L Hansen, MD, MCR
Phone
503494-7500
Email
hansemat@ohsu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Denise Griffiths
Phone
503-494-7015
Email
griffitd@ohsu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthew L Hansen, MD, MCR
Organizational Affiliation
Oregon Health and Science University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University at Buffalo
City
Buffalo
State/Province
New York
ZIP/Postal Code
14261
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brooke Lerner, PhD
Phone
716-645-9726
Email
lerner@buffalo.edu
Facility Name
Mecklenburg County EMS
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28208
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jon Studnek
Phone
704-943-6000
Email
jonst@medic911.com
Facility Name
University of Utah
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84112
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sarah Becker, DO
Phone
801-587-7450
Email
sarah.becker@hsc.utah.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Treating Respiratory Emergencies in Children Study

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