Trial · NCT03296579
Non-invasive Ventilation vs. Standard Therapy for Children Hospitalized With an Acute Exacerbation of Asthma
NCT03296579, Not applicable, Unknown, University of British Columbia
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Non-invasive Ventilation vs. Standard Therapy for Children Hospitalized With an Acute Exacerbation of Asthma. Trials, record NCT03296579. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03296579
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Non-invasive Ventilation vs. Standard Therapy for Children Hospitalized With an Acute Exacerbation of Asthma
- NCT number
- NCT03296579
- Status
- Unknown
- Phases
- Not applicable
- Enrollment
- 100 participants, estimated
- Lead sponsor
- University of British Columbia
- Conditions
- Asthma Acute, Asthma in Children
- Interventions
- BiPAP, CPAP, Ipratropium, Magnesium Sulfate, Aminophylline, Standard steroid dose, hourly salbutamol, oxygen as needed
- First posted
- 2017-09-28
- Last updated
- 2018-05-02
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time to reach a PRAM score of ≤3 | Patients will be followed for the duration of their hospital stay (an estimated average duration of 4 days) | PRAM score includes assessment of oxygen saturations, suprasternal retractions, scalene muscle contraction, air entry and wheezing. |
| Secondary | Time to room air | Patients will be followed for the duration of their hospital stay (an estimated average of 4 days). | Time that oxygen is required |
| Secondary | Total medication use per 12 hr period | Patients will be followed for the duration of their hospital stay (an estimated average of 4 days). | Comparison of total medication use by children in each arm. |
| Secondary | Numbers failing treatment and transferred to ICU | Patients will be followed for the duration of their hospital stay (an estimated average of 4 days). | Number of patients in each group that fail treatment and require transfer to ICU |
| Other | Time to reach FEV1 >80% predicted in those children able to perform pulmonary function tests | Patients will be followed for the duration of their hospital stay (an estimated average of 4 days). | Standard pulmonary function tests can usually be performed by children \>6 years. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers10
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03296579
GET https://conductscience.org/api/trials/v1/NCT03296579/registered