Trial · NCT07901400
Short-Term Enteral Nutrition for Infants With Bronchiolitis in Pediatric Emergency Departments
NCT07901400, Not applicable, Not yet recruiting, Hospices Civils de Lyon
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Short-Term Enteral Nutrition for Infants With Bronchiolitis in Pediatric Emergency Departments. Trials, record NCT07901400. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07901400
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Short-Term Enteral Nutrition for Infants With Bronchiolitis in Pediatric Emergency Departments
- NCT number
- NCT07901400
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 448 participants, estimated
- Lead sponsor
- Hospices Civils de Lyon
- Conditions
- Bronchiolitis, Clinical Phenotype, Nutritionnal Impairment, Short-Term Enteral Nutrition, Emergency Pediatric Care
- Interventions
- Usual inpatient bronchiolitis care, STENP-PER care pathway
- First posted
- 2026-10-28
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Mean total number of hospitalization days through day 14 | Up to day 14 | For each infant, the cumulative number of days spent in conventional hospitalization will include hospitalization immediately following the index pediatric emergency department visit and any subsequent hospitalization or rehospitalization through Day 14 for worsening bronchiolitis or a complication related to management of the index episode. Hospital records and discharge reports will be checked against information obtained during the Day 14 parent telephone call. The mean number of days will be estimated for each study group and compared using a mixed-effects regression model accounting for clustering by center. |
| Secondary | Percentage of infants conventionally hospitalized immediately after the emergency department visit | Day 0 | Percentage of enrolled infants admitted to conventional inpatient care immediately after the pediatric emergency department visit that led to inclusion. The percentage will be compared between study groups using a mixed-effects logistic regression model. |
| Secondary | Percentage of infants transferred to another hospital for immediate hospitalization | Day 0 | Percentage of enrolled infants transferred to another hospital for immediate hospitalization following the index pediatric emergency department visit. The percentage will be compared between study groups using a mixed-effects logistic regression model. |
| Secondary | Parent Satisfaction Index Score Day0 | Day 0 | Parent satisfaction with the infant's care will be assessed using the study-specific standardized questionnaire. It covers information about bronchiolitis and its management, involvement in care, comfort and perceived safety during care, and perceived quality of care. Scores will be summarized by study group. |
| Secondary | Parent Satisfaction Index Score Day14 | Day 14 | Parent satisfaction with the infant's care will be assessed using the study-specific standardized questionnaire. It covers information about bronchiolitis and its management, involvement in care, comfort and perceived safety during care, and perceived quality of care. |
| Secondary | Parent Experience PPE-15 | Day14 | Parent experience assessed by telephone with the 15-item Picker Patient Experience Questionnaire (PPE-15) adapted for pedriatric care. |
| Secondary | Percentage of parents able to recall advice at Day 14 | Day 14 | Percentage of parents who recall the advice provided, assessed by telephone using the study-specific questionnaire. The percentage will be compared between study groups using a mixed-effects logistic regression model. |
| Secondary | Healthcare professional satisfaction score | 2 years, 3 years and 4 years (at the end of each center's first bronchiolitis epidemic season following implementation of the intervention) | Medical and paramedical staff ratings of perceived quality of service to families, department crowding, and team cohesion. Each item is rated on a four-point Likert scale; individual items and their mean will be reported. |
| Secondary | Percentage of infants with at least one adverse event | Up to Day 14 | Percentage of infants experiencing at least one adverse event during the 14 days following inclusion. Events will also be described by nature, severity, and cause category, including disease progression and care organization, after event validation committee review. |
| Secondary | Percentage of infants with at least one adverse serious adverse event | Up to Day 14 | Percentage of infants experiencing at least one serious adverse event during the 14 days following inclusion. Events will also be described by nature, severity, and cause category, including disease progression and care organization, after event validation committee review. |
1 to 10 of 11Source ClinicalTrials.gov
See all 11 registered outcomesOutcomes0
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT07901400
GET https://conductscience.org/api/trials/v1/NCT07901400/registered