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Trial · NCT02285634

The Effect of Intranasal Vasoconstrictor Medications on Hemodynamic Parameters: A Randomized Double-blind, Placebo-controlled Trial.

NCT02285634, Not applicable, Completed, Mayo Clinic; results first posted 2018-10-02

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. The Effect of Intranasal Vasoconstrictor Medications on Hemodynamic Parameters: A Randomized Double-blind, Placebo-controlled Trial. Trials, record NCT02285634. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02285634

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Trial

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

Title
The Effect of Intranasal Vasoconstrictor Medications on Hemodynamic Parameters: A Randomized Double-blind, Placebo-controlled Trial.
NCT number
NCT02285634
Status
Completed
Phases
Not applicable
Enrollment
68 participants, actual
Lead sponsor
Mayo Clinic
Conditions
Epistaxis, Blood Pressure
Interventions
Oxymetazoline 0.05%, Phenylephrine 0.25%, Lidocaine 1% plus epinephrine 1:100,000, Bacteriostatic 0.9% NaCL
First posted
2014-11-07
Last updated
2018-10-02
Results first posted
2018-10-02
Limitations and caveats
The primary limitation was the small sample size as enrollment was markedly more difficult than anticipated.

Source ClinicalTrials.gov

Registered outcomes4

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

ListOutcomeTime frameDescription
PrimaryChange in Mean Arterial Blood Pressurebaseline, 30 minutesChange in mean arterial blood pressure from the baseline measurement
SecondaryChange in Systolic Blood Pressurebaseline, 30 minutesChange from baseline in systolic blood pressure.
SecondaryChange in Diastolic Blood Pressurebaseline, 30 minutesChange from baseline in diastolic blood pressure.
SecondaryChange in Heart Ratebaseline, 30 minutesChange from baseline in heart rate.

Outcomes4

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Mean Arterial Blood Pressurebaseline, 30 minutesmmHgMEAN
SECONDARYChange in Systolic Blood Pressurebaseline, 30 minutesmmHgMEAN
SECONDARYChange in Diastolic Blood Pressurebaseline, 30 minutesmmHgMEAN
SECONDARYChange in Heart Ratebaseline, 30 minutesbeats/minMEAN

Results by group16

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

OutcomeGroupCategoryValueSpreadUnits
Change in Mean Arterial Blood PressureOxymetazoline 0.05%5.1Standard Deviation 6.8mmHg
Change in Mean Arterial Blood PressurePhenylephrine 0.25%6.4Standard Deviation 5.8mmHg
Change in Mean Arterial Blood PressureLidocaine 1% Plus Epinephrine 1:100,0004.6Standard Deviation 8.0mmHg
Change in Mean Arterial Blood PressureBacteriostatic 0.9% NaCL6.5Standard Deviation 5.5mmHg
Change in Systolic Blood PressureOxymetazoline 0.05%7.5Standard Deviation 9.8mmHg
Change in Systolic Blood PressurePhenylephrine 0.25%8.2Standard Deviation 7.2mmHg
Change in Systolic Blood PressureLidocaine 1% Plus Epinephrine 1:100,0003.5Standard Deviation 6.5mmHg
Change in Systolic Blood PressureBacteriostatic 0.9% NaCL8.9Standard Deviation 5.4mmHg
Change in Diastolic Blood PressureOxymetazoline 0.05%5.7Standard Deviation 7.7mmHg
Change in Diastolic Blood PressurePhenylephrine 0.25%7.9Standard Deviation 6.8mmHg

Participant flow12

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDOxymetazoline 0.05%15
Overall StudySTARTEDPhenylephrine 0.25%20
Overall StudySTARTEDLidocaine 1% Plus Epinephrine 1:100,00015
Overall StudySTARTEDBacteriostatic 0.9% Sodium Chloride (NaCL)18
Overall StudyCOMPLETEDOxymetazoline 0.05%15
Overall StudyCOMPLETEDPhenylephrine 0.25%20
Overall StudyCOMPLETEDLidocaine 1% Plus Epinephrine 1:100,00011
Overall StudyCOMPLETEDBacteriostatic 0.9% Sodium Chloride (NaCL)17
Overall StudyNOT COMPLETEDOxymetazoline 0.05%0
Overall StudyNOT COMPLETEDPhenylephrine 0.25%0

Adverse events16

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherNasal PainGeneral disordersOxymetazoline 0.05%2152
otherNasal PainGeneral disordersPhenylephrine 0.25%2202
otherNasal PainGeneral disordersLidocaine 1% Plus Epinephrine 1:100,0000110
otherNasal PainGeneral disordersBacteriostatic 0.9% NaCL0170
otherEye wateringEye disordersOxymetazoline 0.05%1151
otherEye wateringEye disordersPhenylephrine 0.25%0200
otherEye wateringEye disordersLidocaine 1% Plus Epinephrine 1:100,0000110
otherEye wateringEye disordersBacteriostatic 0.9% NaCL0170
otherDizinessGeneral disordersOxymetazoline 0.05%0150
otherDizinessGeneral disordersPhenylephrine 0.25%1201

Adverse event totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityOxymetazoline 0.05%015
Total, all-cause mortalityPhenylephrine 0.25%020
Total, all-cause mortalityLidocaine 1% Plus Epinephrine 1:100,000011
Total, all-cause mortalityBacteriostatic 0.9% NaCL017
Total, other adverse eventsOxymetazoline 0.05%415
Total, other adverse eventsPhenylephrine 0.25%320
Total, other adverse eventsLidocaine 1% Plus Epinephrine 1:100,000011
Total, other adverse eventsBacteriostatic 0.9% NaCL217
Total, serious adverse eventsOxymetazoline 0.05%015
Total, serious adverse eventsPhenylephrine 0.25%020

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
30195946BACKGROUND

Source PubMed

Grants1

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
UL1TR000135Mayo Clinic Center for Clinical and Translational Science (CCaTS)KHOSLA, SUNDEEPMAYO CLINIC ROCHESTERNATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES2012 to 2015

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/NCT02285634

GET https://conductscience.org/api/trials/v1/NCT02285634/registered