Pediatric Intubation Simulations With Bougie
NCT07915661, Not applicable, Enrolling by invitation, University of Texas at Austin
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Pediatric Intubation Simulations With Bougie | ClinicalTrials.gov |
| NCT number | NCT07915661 | ClinicalTrials.gov |
| Status | Enrolling by invitation | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 50 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | University of Texas at Austin | ClinicalTrials.gov |
| Conditions | Difficult Airway Intubation | ClinicalTrials.gov |
| Interventions | Simulation-Based Bougie-Assisted Pediatric Intubation Training | ClinicalTrials.gov |
| First posted | 2026-11-04 | ClinicalTrials.gov |
| Last updated | 2026-11-04 | ClinicalTrials.gov |
Registered outcomes 4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Time to Successful Bougie-Assisted Intubation | During the simulation session (approximately 30 minutes). | Time (in seconds) from insertion of the laryngoscope into the mouth until successful endotracheal intubation and removal of the laryngoscope. Time will be measured for each of two simulated difficult pediatric airway scenarios using video recordings. Intubation times will be compared between scenarios and randomized sequences. | ClinicalTrials.gov |
| Secondary | Change in Provider Comfort and Confidence With Bougie-Assisted Intubation | Immediately before and after simulation-based training (approximately 60 minutes). | Change in self-reported comfort and confidence with bougie-assisted pediatric intubation from pre-simulation to immediately post-simulation, as measured by participant surveys. Responses will be compared to assess changes following simulation-based training. | ClinicalTrials.gov |
| Secondary | Retention of Provider Comfort and Confidence at 6 Months | Baseline, immediately post-simulation, and 6 months post-simulation. | Change in self-reported comfort with bougie-assisted pediatric intubation from baseline to immediately following simulation-based training. Comfort will be measured using a 5-point Likert scale, with higher scores indicating greater comfort. Changes in comfort scores will be assessed by comparing pre-simulation and post-simulation survey responses. | ClinicalTrials.gov |
| Secondary | Frequency of Clinical Bougie Use Following Simulation-Based Training | Six months following simulation-based training. | Participants will report the number of times they have used a bougie during clinical intubation procedures in the 6 months following simulation-based training. The outcome will be measured as the self-reported number of bougie-assisted intubations per participant during the follow-up period. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 4
The papers the trial lists on ClinicalTrials.gov.
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)