Trial · NCT01782560
Laryngomalacia Study
NCT01782560, Phase 1, Withdrawn, Children's & Women's Health Centre of British Columbia
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Laryngomalacia Study. Trials, record NCT01782560. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01782560
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Laryngomalacia Study
- NCT number
- NCT01782560
- Status
- Withdrawn
- Phases
- Phase 1
- Enrollment
- 0 participants, actual
- Lead sponsor
- Children's & Women's Health Centre of British Columbia
- Conditions
- Laryngomalacia
- Interventions
- Omeprazole, Placebo
- First posted
- 2013-02-04
- Last updated
- 2015-07-30
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Laryngomalacia Symptom Score | Change from baseline and at end of study (baseline and 8 weeks) | This score is a disease-specific quality of life measure for laryngomalacia. Each of the symptoms that can occur in laryngomalacia are scored as present (1) or absent (0) as follows - inspiratory stridor, suprasternal retraction, substernal retraction, feeding difficulty, choking, post-feeding vomit, failure to thrive (i.e. poor weight gain with deviation from the normal growth curve), and cyanosis. Therefore for each patient, a total symptom score is calculated (8 = all symptoms, 0 = no symptoms). |
| Secondary | Caring For a Child with Laryngomalacia Family Impact Questionnaire | Change from baseline and at end of study (baseline and 8 weeks) | |
| Secondary | Revised Infant Gastro-Esophageal Reflux Questionnaire | Change from baseline and at end of study (baseline and 8 weeks) | |
| Secondary | Reflux Finding Score | Change from baseline and at end of study (baseline and 8 weeks) | |
| Secondary | End of treatment 24-hour double-probe pH monitoring | Change from baseline and at end of study (baseline and 8 weeks) | |
| Secondary | Weight | Change from baseline, to half-way point and at end of study (baseline, 4 weeks and 8 weeks) |
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.
Papers18
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/NCT01782560
GET https://conductscience.org/api/trials/v1/NCT01782560/registered