Trial · NCT05557344
Oral vs IV Acetaminophen for Long-bone Fracture in Children
NCT05557344, Phase 4, Unknown, Dr. Niina Kleiber
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Oral vs IV Acetaminophen for Long-bone Fracture in Children. Trials, record NCT05557344. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05557344
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Oral vs IV Acetaminophen for Long-bone Fracture in Children
- NCT number
- NCT05557344
- Status
- Unknown
- Phases
- Phase 4
- Enrollment
- 20 participants, estimated
- Lead sponsor
- Dr. Niina Kleiber
- Conditions
- Pain
- Interventions
- Acetaminophen IV, Acetaminophen
- First posted
- 2022-09-28
- Last updated
- 2022-09-28
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in pain scores | During 24h (starting with the first dose of study drug) | Pain scores within the first 24 hours following initiation of study drug, using the scales Face, Legs, Activity, Cry, Consolability (FLACC, 0-2 per item for a total of 10, 10 being the worst pain) and verbal numerical rating (VNR, 0-10, 10 being the worst pain). |
| Primary | Difference in quantity of rescue opioids | During 24h (starting with the first dose of study drug) | Quantity of rescue opioids (morphine equivalent in mg/kg) within the first 24 hours following initiation of study drug |
| Secondary | Adverse events | During 24h (starting with the first dose of study drug) | Any other adverse effect whether or not attributed to the study drug will be carefully recorded. Opioid-related adverse effects will be recorded (pruritus, time to first bowel movement, nausea (self-reported), vomiting, days of bladder catheterization, oxygen supplementation, episodes of respiratory depression (\< 10/min in children older than 5 years), use of diphenhydramine, naloxone, antiemetics, laxatives). |
| Secondary | Determination of oral bioavailability | During 24 hours after the first dose of study drug | Blood level of acetaminophen will be determined |
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.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 34676011 | BACKGROUND |
Source PubMed
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/NCT05557344
GET https://conductscience.org/api/trials/v1/NCT05557344/registered