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Trial · NCT00732381

Study of Nasonex in the Relief of Nasal Congestion in Patients With Seasonal Allergic Rhinitis (Study P05529)

NCT00732381, Phase 3, Completed, Organon and Co; results first posted 2009-11-13

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Study of Nasonex in the Relief of Nasal Congestion in Patients With Seasonal Allergic Rhinitis (Study P05529). Trials, record NCT00732381. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00732381

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Trial

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

Title
Study of Nasonex in the Relief of Nasal Congestion in Patients With Seasonal Allergic Rhinitis (Study P05529)
NCT number
NCT00732381
Status
Completed
Phases
Phase 3
Enrollment
351 participants, actual
Lead sponsor
Organon and Co
Conditions
Allergic Rhinitis
Interventions
Mometasone furoate nasal spray (MFNS), Matching placebo nasal spray
First posted
2008-08-12
Last updated
2024-05-21
Results first posted
2009-11-13

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryThe Change From Baseline in Average AM/PM PRIOR Nasal Congestion Score Over 15 Days15 days of treatmentNasal congestion was scored on a scale of 0 = none, 1 = mild, 2 = moderate, and 3 = severe symptoms. PRIOR (the subject's status over the previous 12 hours \[reflective\])
SecondaryThe Change From Baseline in Average AM/PM PRIOR Total Nasal Symptom Score Over 15 Days15 days of treatment
Total nasal symptom score (TNSS) is a composite of 4 symptoms, each is scored on a scale of 0 = none, 1 = mild, 2 = moderate, 3 = severe. The total can range from 0 to 12. PRIOR (the subject's status over the previous 12 hours \[reflective\])

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYThe Change From Baseline in Average AM/PM PRIOR Nasal Congestion Score Over 15 Days15 days of treatmentThe standard deviation is pooled.Units on a scaleLEAST_SQUARES_MEAN
SECONDARYThe Change From Baseline in Average AM/PM PRIOR Total Nasal Symptom Score Over 15 Days15 days of treatmentUnits on a scaleLEAST_SQUARES_MEAN

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
The Change From Baseline in Average AM/PM PRIOR Nasal Congestion Score Over 15 DaysMometasone Furoate Nasal Spray-0.64Standard Deviation 0.52Units on a scale
The Change From Baseline in Average AM/PM PRIOR Nasal Congestion Score Over 15 DaysPlacebo Nasal Spray-0.49Standard Deviation 0.52Units on a scale
The Change From Baseline in Average AM/PM PRIOR Total Nasal Symptom Score Over 15 DaysMometasone Furoate Nasal Spray-2.68Standard Deviation 2.01Units on a scale
The Change From Baseline in Average AM/PM PRIOR Total Nasal Symptom Score Over 15 DaysPlacebo Nasal Spray-1.85Standard Deviation 2.01Units on a scale

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDMometasone Furoate Nasal Spray176
Overall StudySTARTEDPlacebo Nasal Spray175
Overall StudyCOMPLETEDMometasone Furoate Nasal Spray174
Overall StudyCOMPLETEDPlacebo Nasal Spray174
Overall StudyNOT COMPLETEDMometasone Furoate Nasal Spray2
Overall StudyNOT COMPLETEDPlacebo Nasal Spray1

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 totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMometasone Furoate Nasal Spray
Total, all-cause mortalityPlacebo Nasal Spray
Total, other adverse eventsMometasone Furoate Nasal Spray0176
Total, other adverse eventsPlacebo Nasal Spray0175
Total, serious adverse eventsMometasone Furoate Nasal Spray0176
Total, serious adverse eventsPlacebo Nasal Spray0175

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
21439168RESULT

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 comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Mometasone Furoate Nasal Spray vs Placebo Nasal Spray: serious adverse events

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/NCT00732381

GET https://conductscience.org/api/trials/v1/NCT00732381/registered