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Trial · NCT02927834

Oral Steroids in Chronic Rhinosinusitis Without Nasal Polyps

NCT02927834, Not applicable, Completed, Loma Linda University; results first posted 2020-12-29

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Oral Steroids in Chronic Rhinosinusitis Without Nasal Polyps. Trials, record NCT02927834. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02927834

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Trial

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

Title
Oral Steroids in Chronic Rhinosinusitis Without Nasal Polyps
NCT number
NCT02927834
Status
Completed
Phases
Not applicable
Enrollment
24 participants, actual
Lead sponsor
Loma Linda University
Conditions
Sinusitis
Interventions
6 day Prednisone, Augmentin, 21 day Prednisone
First posted
2016-10-07
Last updated
2020-12-29
Results first posted
2020-12-29

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimarySinonasal Outcome Test (SNOT 20)4 weeks post treatmentSinonasal outcome test to access nasal/sinus symptoms. 20 questions, each question scored 0-5. 0 meaning no symptoms, 5 worse. 0- 100 total with lower number meaning better outcome
PrimaryNasal Endoscopy4 weeks post treatmentPhysical exam findings of the nasal cavity. Scored 0-12. Lower score is better
PrimaryCT Scan Changes4 week post treatmentCT scan of the sinuses, Lund Mackay score to access severity of sinus disease on CT scan. Scored on scale 0-20 with lower score better.

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYSinonasal Outcome Test (SNOT 20)4 weeks post treatmentScore out of total 100MEAN
PRIMARYNasal Endoscopy4 weeks post treatmentscore out of total 12MEAN
PRIMARYCT Scan Changes4 week post treatmentscore out of total 20MEAN

Results by group9

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

OutcomeGroupCategoryValueSpreadUnits
Sinonasal Outcome Test (SNOT 20)Antibiotic Only50.3395% Confidence Interval -2.21 to 56.29Score out of total 100
Sinonasal Outcome Test (SNOT 20)Augmentin With 6 Day Steroid53.1495% Confidence Interval 1.79 to 59.92Score out of total 100
Sinonasal Outcome Test (SNOT 20)Augmentin With 21 Day Steroid3795% Confidence Interval 2.85 to 39Score out of total 100
Nasal EndoscopyAntibiotic Only2.5595% Confidence Interval -2.197 to 2.974score out of total 12
Nasal EndoscopyAugmentin With 6 Day Steroid3.0095% Confidence Interval 1.793 to 3.492score out of total 12
Nasal EndoscopyAugmentin With 21 Day Steroid2.1695% Confidence Interval -2.37 to 3.37score out of total 12
CT Scan ChangesAntibiotic Only10.3395% Confidence Interval 8.15 to 11.3score out of total 20
CT Scan ChangesAugmentin With 6 Day Steroid1195% Confidence Interval 7.68 to 11.8score out of total 20
CT Scan ChangesAugmentin With 21 Day Steroid11.8395% Confidence Interval 5.13 to 13.15score out of total 20

Participant flow9

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDAntibiotic Only8
Overall StudySTARTEDAugmentin With 6 Day Steroid8
Overall StudySTARTEDAugmentin With 21 Day Steroid8
Overall StudyCOMPLETEDAntibiotic Only7
Overall StudyCOMPLETEDAugmentin With 6 Day Steroid6
Overall StudyCOMPLETEDAugmentin With 21 Day Steroid6
Overall StudyNOT COMPLETEDAntibiotic Only1
Overall StudyNOT COMPLETEDAugmentin With 6 Day Steroid2
Overall StudyNOT COMPLETEDAugmentin With 21 Day Steroid2

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 totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityAntibiotic Only07
Total, all-cause mortalityAugmentin With 6 Day Steroid06
Total, all-cause mortalityAugmentin With 21 Day Steroid06
Total, other adverse eventsAntibiotic Only07
Total, other adverse eventsAugmentin With 6 Day Steroid06
Total, other adverse eventsAugmentin With 21 Day Steroid06
Total, serious adverse eventsAntibiotic Only07
Total, serious adverse eventsAugmentin With 6 Day Steroid06
Total, serious adverse eventsAugmentin With 21 Day Steroid06

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/NCT02927834

GET https://conductscience.org/api/trials/v1/NCT02927834/registered