Placement of Nasogastric Tubes for Gastric Decompression in Patients With Bronchiolitis

Arkansas Children's Hospital Research Institute

Status: Enrolling

Conditions: Bronchiolitis

Treatments: Device: Nasogastric tube placement

Study type: Interventional

Funder types: Other

Identifiers

NCT04480970

IRB 261122

Details and patient eligibility

About

This study aims to evaluate whether placing nasogastric tubes for gastric decompression improves respiratory distress for patients with bronchiolitis who are receiving oxygen via high-flow nasal cannula.

Full description

All patients will be consented per IRB procedure. The study will be a prospective study. Study participants will be enrolled after placement on high flow nasal cannula. The respiratory therapist or study staff will use a bronchiolitis scoring tool, the Marlais Risk of Admission Score, to assess the respiratory status of patients after placement on high flow nasal cannula, and prior to placement of NG tube to establish a baseline measurement. This tool includes the following components: respiratory rate, oxygen saturation, heart rate, age, and length of illness. An NG tube will then be placed. Thirty minutes and sixty minutes after placement of the NG tube, the respiratory therapist or study team will again use this scoring tool to assess the respiratory status of the patient. After 60 minutes the study will be concluded. As subject will be requiring oxygen use, admission to an inpatient unit is required. The NG tube will be removed at the discretion of the provider or the admitting physician, who may choose to keep it in at their discretion.

Enrollment: 60 estimated patients

Sex: All

Ages: 1 day to 23 months old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Diagnosis of bronchiolitis by the attending physician
• On high flow nasal cannula (4 liters or greater)
• Ages 0 months to 23 months

Exclusion criteria

• Diagnosis of bacterial pneumonia
• History of cranio-facial anomalies
• History of congenital heart disease
• History of G-tube dependence
• History of short gut syndrome
• History of tracheostomy or current tracheostomy

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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60 participants in 1 patient group

Nasogastric tube placement

Experimental group

Treatment:

Device: Nasogastric tube placement