Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01871857 · ClinicalTrials.gov registry record · Phase 4

7% Hypertonic Saline for Acute Bronchiolitis

A Phase 4 study, sponsored by Le Bonheur Children's Hospital.

Completed
Registry status
Phase 4
Development phase
101
Enrollment target

NCT01871857: Completed Phase 4 study, sponsored by Le Bonheur Children's Hospital.

NCT01871857 is a Phase 4 study that has completed, run by Le Bonheur Children's Hospital. The registered enrollment target is 101 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01871857, a Phase 4 study, has completed, sponsored by Le Bonheur Children's Hospital.

COMPLETED
Registry status
Phase 4
Development phase
101 participants
Enrollment target

Study Summary

Research suggests that hypertonic saline may improve mucous flow in infants with acute bronchiolitis. Data suggest a trend favoring reduced length of hospital stay and improved pulmonary scores with increasing concentration of nebulized solution to 3% and 5% saline as compared to 0.9% saline mixed with epinephrine. To our knowledge, 7% hypertonic saline has not been previously investigated. OUr hypothesis was that 7% hypertonic saline would improve bronchiolitis severity scores and admission rate.

Primary Outcome

Bronchiolitis severity scores were recorded prior to administering aerosols, after administering the aerosol, and again once the treating clinician determined the final disposition of the patient. After a 4-h observation period, the treating clinician determined patient disposition. If admitted, the patient continued to receive aerosols containing the same designated medication every 6 h until discharge or 24 h after the admission. Bronchiolitis severity scores were obtained before and after ea

Interventions

  • DRUG Hypertonic saline and epinephrine
  • DRUG Normal saline and epinephrine

Trial Details

FieldValue
Enrollment Target 101 participants
Start Date 2010-11
Est. Completion 2012-08
Phase Phase 4
Le Bonheur Children's Hospital

14 total trials

What the finished NCT01871857 record still lists

NCT01871857 is an interventional study that assigns participants to a tested intervention. The registered 101 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower).

The record links to 0 conditions, and to 2 interventions - of which Hypertonic saline and epinephrine is the first listed.

NCT01871857 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01871857 about?

NCT01871857 is a clinical study titled "7% Hypertonic Saline for Acute Bronchiolitis". Research suggests that hypertonic saline may improve mucous flow in infants with acute bronchiolitis. Data suggest a trend favoring reduced length of hospital stay and improved pulmonary scores with increasing concentration of nebulized solution to 3% and 5% saline as compared to 0.9% saline mixed w...

What is the current status of trial NCT01871857?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 101 participants. The study started on 2010-11. Estimated completion is 2012-08.

What interventions are being tested in trial NCT01871857?

The interventions under investigation include: Hypertonic saline and epinephrine (DRUG), Normal saline and epinephrine (DRUG).

Who is sponsoring clinical trial NCT01871857?

This trial is sponsored by Le Bonheur Children's Hospital, which has 14 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01871857's enrollment target sits among peer trials

101 766th of 2000 higher than 1,231 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04033497 · 101 participants · NA

    Treatment Response Assessment Maps to Delineate Necrosis From Tumor After Stereotactic Radiation in Brain Metastases

  • NCT05111574 · 101 participants · Phase 2

    Using Nivolumab Alone or With Cabozantinib to Prevent Mucosal Melanoma Return After Surgery

  • NCT05984680 · 101 participants

    COPD Care Pathway Among Patients With Cancer

  • NCT06266299 · 101 participants · Phase 1

    A Study of KK2269 in Adult Participants With Solid Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01871857, the US trial registry maintained by the National Library of Medicine. NCT01871857 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.