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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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03647397
Enrollment
274
Registered
2018-08-27
Start date
2018-08-08
Completion date
2018-12-31
Last updated
2019-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma, Pneumonia, Respiratory Distress Syndrome

Keywords

asthma, environmental intervention, respiratory distress, pediatric hospitalization, pneumonia, bronchiolitis

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.

Detailed description

The goal of this study is to assess whether using PECO to purify air in a hospital can improve health outcomes for pediatric patients with respiratory distress. The results of this study will be used in three primary ways: 1. As evidence to support an installation of PECO in hospital HVAC systems to improve the standard of care for patients with respiratory distress 2. Towards dissemination efforts through publication in a peer-reviewed journal and presentation at national and international conferences 3. For informing healthcare providers and stakeholders There are no plans to repeat this study with other hospital partners

Interventions

DEVICEPhoto Electrochemical Oxidation (PECO) for Air Purification

PECO air purifiers from Molekule will be placed in every patient room. Health metrics will be tracked for patients whose diagnosis is respiratory distress.

Sponsors

Mercy Health System
CollaboratorNETWORK
Molekule
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

All pediatric patients who are admitted to the Mercyhealth Hospital - Rockton Avenue following the Start Date and have infectious or non-infectious respiratory distress as defined by the following ICD codes will be included in the study: * 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

Exclusion criteria

* Any patient admitted to the NICU * Patients in the ER only * Any patient with non-respiratory conditions * Adults

Design outcomes

Primary

MeasureTime frameDescription
Length of stay5 monthsTotal length of hospital stay for patient

Secondary

MeasureTime frameDescription
Readmission rate1 monthsRate of readmission within 30 days of discharge

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026