Efficacy Of Combined Nebulized Hypertonic Saline and Chest Percussion Therapy in Acute Viral Bronchiolitis

Last updated: June 2, 2025
Sponsor: NYU Langone Health
Overall Status: Completed

Phase

4

Condition

Bronchitis (Pediatric)

Respiratory Syncytial Virus (Rsv) Infection

Treatment

Chest percussion cups

Nebulized 3% sodium chloride solution

Clinical Study ID

NCT06441162
23-01357
  • Ages < 24
  • All Genders

Study Summary

This study will examine the efficacy of combined nebulized hypertonic saline with chest percussion therapy in patients age 0 to 24 months admitted to the general inpatient pediatrics unit with acute bronchiolitis. 3% nebulized hypertonic saline treatments combined with 3 minutes of chest percussion therapy will be administered every 6 hours of patients selected for the study.

Eligibility Criteria

Inclusion

Inclusion Criteria:

In order to be eligible to participate in this study (experimental arm), an individual must meet all of the following criteria:

  • Age 0 to 24 months

  • Admitted to the general inpatient pediatrics unit

  • Has a diagnosis of acute bronchiolitis

  • Receiving supplemental oxygen support

Data collected for the control arm will be obtained via retrospective chart review for patients meeting the following inclusion criteria:

  • Age 0 to 24 months

  • Admitted to the general inpatient pediatrics unit

  • Has a diagnosis of acute bronchiolitis

  • Receiving supplemental oxygen support

Exclusion

Exclusion Criteria:

An individual who meets any of the following criteria will be excluded from participation in this study:

  • Admitted to the pediatric intensive care unit

  • Has an underlying pre-existing condition that may affect the respiratory system (includes bronchopulmonary dysplasia, reactive airways disease, asthma, restrictivelung diseases, other chronic lung diseases, etc.)

  • Has other comorbid conditions upon admission that may affect the respiratory system (includes pneumonia or other bacterial or fungal lung infections, acute exacerbationof reactive airways disease, acute exacerbation of asthma, pulmonary edema, pleuraleffusion, etc.)

  • Has an absolute contraindication to nebulized 3% hypertonic saline, for example, ahistory of an allergic or anaphylactic reaction

  • Is receiving other respiratory treatments such as bronchodilator treatments (i.e.albuterol or levalbuterol)

  • Is receiving other adjuvant therapy such as antibiotics, antivirals,glucocorticoids, corticosteroids, or diuretics

A potential study subject in the control arm via retrospective chart review who meets any of the following criteria will be excluded from this study:

  • Admitted to the pediatric intensive care unit

  • Has an underlying pre-existing condition that may affect the respiratory system (includes bronchopulmonary dysplasia, reactive airways disease, asthma, restrictivelung diseases, other chronic lung diseases, etc.)

  • Has other comorbid conditions upon admission that may affect the respiratory system (includes pneumonia or other bacterial or fungal lung infections, acute exacerbationof reactive airways disease, acute exacerbation of asthma, pulmonary edema, pleuraleffusion, etc.)

  • Has an absolute contraindication to nebulized 3% hypertonic saline, for example, ahistory of an allergic or anaphylactic reaction

  • Is receiving other respiratory treatments such as bronchodilator treatments (i.e.albuterol or levalbuterol)

  • Is receiving other adjuvant therapy such as antibiotics, antivirals,glucocorticoids, corticosteroids, or diuretics

Study Design

Total Participants: 75
Treatment Group(s): 2
Primary Treatment: Chest percussion cups
Phase: 4
Study Start date:
July 15, 2024
Estimated Completion Date:
May 15, 2025

Connect with a study center

  • NYU Langone Health

    Mineola, New York 11501
    United States

    Site Not Available

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