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NCT04599101 · ClinicalTrials.gov registry record · NA

Nasal Suction in Infants With Bronchiolitis Using a NoseFrida vs. Bulb Syringe

A NA study, sponsored by Corewell Health East.

Terminated
Registry status
NA
Development phase
21
Enrollment target

NCT04599101: Clinical Trial NA study, sponsored by Corewell Health East.

NCT04599101 is a NA study that was terminated before completion, run by Corewell Health East. The registered enrollment target is 21 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04599101, a NA study, was terminated before completion, sponsored by Corewell Health East.

TERMINATED
Registry status
NA
Development phase
21 participants
Enrollment target

Study Summary

This research study will evaluate the difference in effectiveness of nasal suction between two different suction devices (NoseFrida and bulb syringe) in infants that have bronchiolitis. Bronchiolitis (a virus infection that goes into the lungs, which subsequently causes difficulty breathing, difficulty sleeping, and difficulty eating and drinking in children) is a common infection in young children. The caregiver-participants will be supplied with a suction devices (either NoseFrida and bulb syringe suction). The device should be used to clear nasal secretions as needed following discharge from the Emergency Center. The participants will be asked to use either a NoseFrida device or a bulb syringe. Caregivers will monitor how well their baby is breathing, eating/drinking, sleeping and how many times the baby has been seen by a medical provider in the 5 days post discharge from the Emergency Center. Post discharge, caregivers will complete a REDCAP survey asking questions about how their baby has been doing over the first 5 days following hospital discharge. REDCAP survey will be sent day 5 and again on day 7 if not completed. This completes study involvement.

Primary Outcome

Number of emergency room visits for the same respiratory illness within 5 days following discharge, measured via caregiver response on Redcap survey

Interventions

  • DEVICE Nose Frida nasal suction device
  • DEVICE Bulb syringe nasal suction device

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2020-11-21
Est. Completion 2023-04-18
Phase NA
Corewell Health East

106 total trials

Why NCT04599101 stopped before completion

NCT04599101 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Nose Frida nasal suction device is the first listed.

NCT04599101 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04599101 about?

NCT04599101 is a clinical study titled "Nasal Suction in Infants With Bronchiolitis Using a NoseFrida vs. Bulb Syringe". This research study will evaluate the difference in effectiveness of nasal suction between two different suction devices (NoseFrida and bulb syringe) in infants that have bronchiolitis. Bronchiolitis (a virus infection that goes into the lungs, which subsequently causes difficulty breathing, difficu...

What is the current status of trial NCT04599101?

This trial is currently terminated. It is a NA study. The enrollment target is 21 participants. The study started on 2020-11-21. Estimated completion is 2023-04-18.

What interventions are being tested in trial NCT04599101?

The interventions under investigation include: Nose Frida nasal suction device (DEVICE), Bulb syringe nasal suction device (DEVICE).

Who is sponsoring clinical trial NCT04599101?

This trial is sponsored by Corewell Health East, which has 106 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04599101's enrollment target sits among peer trials

21 1762nd of 2000 higher than 233 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

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Source: ClinicalTrials.gov NCT04599101, the US trial registry maintained by the National Library of Medicine. NCT04599101 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.