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Trial · NCT02453841

Prospective Hemodynamic and Pharmacokinetic Analysis of Oxymetazoline Absorption

NCT02453841, Not applicable, Completed, Richard Cartabuke; results first posted 2018-09-18

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Prospective Hemodynamic and Pharmacokinetic Analysis of Oxymetazoline Absorption. Trials, record NCT02453841. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02453841

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Prospective Hemodynamic and Pharmacokinetic Analysis of Oxymetazoline Absorption
NCT number
NCT02453841
Status
Completed
Phases
Not applicable
Enrollment
30 participants, actual
Lead sponsor
Richard Cartabuke
Conditions
Adenoidectomy, Functional Endoscopic Sinus Surgery (FESS), Turbinate Surgery
Interventions
Oxymetazoline
First posted
2015-05-27
Last updated
2018-09-18
Results first posted
2018-09-18

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBlood Pressure Following Oxymetazoline Administration5 - 150 mins. after administrationBlood pressure was recorded at 5 minute intervals until discharge from the post-anesthesia care unit (PACU) or the final blood draw (150 mins. after administration), whichever came first.
PrimaryHeart Rate Following Oxymetazoline Administration.5 - 150 mins. after administrationHeart rate was recorded at 5 minute intervals until discharge from the post-anesthesia care unit (PACU) or the final blood draw (150 mins. after administration), whichever came first.
SecondaryEase of HemostasisintraoperativeA six point scale (very easy, easy, usual, some effort, difficult, extremely difficult) completed by the surgeon at the end of surgery.
SecondaryAmount of BleedingintraoperativeA four point scale (none, minimal, moderate/diffuse ooze, severe/brisk) completed by the surgeon after removal of the oxymetazoline soaked pledgets.

Outcomes4

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYBlood Pressure Following Oxymetazoline Administration5 - 150 mins. after administrationmmHgMEAN
PRIMARYHeart Rate Following Oxymetazoline Administration.5 - 150 mins. after administrationbeats per minuteMEAN
SECONDARYEase of HemostasisintraoperativeParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYAmount of BleedingintraoperativeParticipantsCOUNT_OF_PARTICIPANTS

Results by group10

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Blood Pressure Following Oxymetazoline AdministrationChildren Undergoing ENT SurgerySystolic blood pressure102Standard Deviation 16mmHg
Blood Pressure Following Oxymetazoline AdministrationChildren Undergoing ENT SurgeryDiastolic blood pressure53Standard Deviation 17mmHg
Blood Pressure Following Oxymetazoline AdministrationChildren Undergoing ENT SurgeryMean arterial pressure65Standard Deviation 15mmHg
Heart Rate Following Oxymetazoline Administration.Children Undergoing ENT Surgery98Standard Deviation 22beats per minute
Ease of HemostasisChildren Undergoing ENT SurgeryVery Easy10Participants
Ease of HemostasisChildren Undergoing ENT SurgeryEasy9Participants
Ease of HemostasisChildren Undergoing ENT SurgeryUsual8Participants
Amount of BleedingChildren Undergoing ENT SurgeryNone11Participants
Amount of BleedingChildren Undergoing ENT SurgeryMinimal11Participants
Amount of BleedingChildren Undergoing ENT SurgeryModerate5Participants

Participant flow3

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDChildren Undergoing ENT Surgery30
Overall StudyCOMPLETEDChildren Undergoing ENT Surgery27
Overall StudyNOT COMPLETEDChildren Undergoing ENT Surgery3

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 totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityChildren Undergoing ENT Surgery030
Total, other adverse eventsChildren Undergoing ENT Surgery030
Total, serious adverse eventsChildren Undergoing ENT Surgery030

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT02453841

GET https://conductscience.org/api/trials/v1/NCT02453841/registered