PECO Air Purification in Hospital Rooms to Improve Health Outcomes for Pediatric Respiratory Distress
Use of PECO Air Purification in Hospital Rooms to Improve Health Outcomes for Pediatric Respiratory Distress
1 other identifier
interventional
274
1 country
1
Brief Summary
This study will investigate the efficacy of a novel air purification technology, Photo Electrochemical Oxidation (PECO), has on pediatric patients hospitalized for respiratory distress. The study will take place at Mercyhealth Hospital - Rockton Avenue where all 23 pediatric rooms will be outfitted with portable PECO air purifying units. The main outcomes are the length of stay and progression to ICU, which will be compared with historical controls.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable asthma
Started Aug 2018
Shorter than P25 for not_applicable asthma
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 8, 2018
CompletedFirst Submitted
Initial submission to the registry
August 20, 2018
CompletedFirst Posted
Study publicly available on registry
August 27, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2018
CompletedMay 17, 2019
May 1, 2019
5 months
August 20, 2018
May 15, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Length of stay
Total length of hospital stay for patient
5 months
Secondary Outcomes (1)
Readmission rate
1 months
Study Arms (1)
PECO
EXPERIMENTALAll pediatric patients admitted for respiratory distress will have the intervention of Photo Electrochemical Oxidation (PECO) for Air Purification.
Interventions
PECO air purifiers from Molekule will be placed in every patient room. Health metrics will be tracked for patients whose diagnosis is respiratory distress.
Eligibility Criteria
You may qualify if:
- J00-J06: Acute upper respiratory infections
- J09-J18: Influenza and pneumonia
- J20-J22: Other acute lower respiratory infections
- J30-J39: Other diseases of upper respiratory tract
- J40-J47: Chronic lower respiratory diseases
- J60-J70: Lung diseases due to external agents
- J80-J84: Other respiratory diseases principally affecting the interstitium
- J85-J86: Suppurative and necrotic conditions of the lower respiratory tract
- J90-J94: Other diseases of the pleura
- J95-J95: Intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified
You may not qualify if:
- Any patient admitted to the NICU
- Patients in the ER only
- Any patient with non-respiratory conditions
- Adults
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Molekulelead
- Mercy Health Systemcollaborator
Study Sites (1)
Mercyhealth Hospital - Rockton Avenue
Rockford, Illinois, 61103, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Nikhil Rao
Molekule
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 20, 2018
First Posted
August 27, 2018
Study Start
August 8, 2018
Primary Completion
December 31, 2018
Study Completion
December 31, 2018
Last Updated
May 17, 2019
Record last verified: 2019-05
Data Sharing
- IPD Sharing
- Will not share