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Trial · NCT02479451

Helping Olfaction and Nutrition On Renal Replacement

NCT02479451, Phase 2, Completed, Massachusetts General Hospital; results first posted 2024-01-09

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Helping Olfaction and Nutrition On Renal Replacement. Trials, record NCT02479451. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02479451

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Trial

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

Title
Helping Olfaction and Nutrition On Renal Replacement
NCT number
NCT02479451
Status
Completed
Phases
Phase 2
Enrollment
7 participants, actual
Lead sponsor
Massachusetts General Hospital
Conditions
End Stage Renal Disease, Olfactory Disorders
Interventions
Theophylline
First posted
2015-06-24
Last updated
2024-01-09
Results first posted
2024-01-09

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimaryChange From Baseline in Smell Identification Test Score at 6 WeeksBaseline and every 2 weeks for 6 weeks
Smell identification test is a validated 40-item scratch and sniff smell identification test that was administered by study investigators. Scores on this test scale range between 0 (minimum) to 40 (maximum). Higher score indicates better ability for smell identification. Total scores are reported on this scale (no sub-scales). The unit is score on this scale.
PrimaryChange From Baseline in Smell Threshold Test Score at 6 WeeksBaseline and every 2 weeks for 6 weeks
This test determined the lowest concentration of an odor compound that is perceivable by study participants. Scores on this test scale range between -2 and -10. Higher score indicates higher smell detection threshold (i.e. worse ability to smell). Total scores are reported on this scale (no sub-scales). The unit is score on this scale.
SecondaryChange From Baseline in Plasma Theophylline Level at 6 WeeksBaseline and every 2 weeks for 6 weeks
Plasma levels of theophylline were measured using fluorescence polarization technique. Minimum level will be 0 microgram/mL and maximum assay limit is 40 microgram/mL. Higher levels indicate increased systemic exposure to theophylline. Units on scale are microgram/mL.

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline in Smell Identification Test Score at 6 WeeksBaseline and every 2 weeks for 6 weeksunits on a scaleMEAN
PRIMARYChange From Baseline in Smell Threshold Test Score at 6 WeeksBaseline and every 2 weeks for 6 weekschange in score on the scaleMEAN
SECONDARYChange From Baseline in Plasma Theophylline Level at 6 WeeksBaseline and every 2 weeks for 6 weeksSerum theophylline levels assessed at every follow-up were undetectable throughout the study period in all participants.microgram/mLMEAN

Results by group3

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in Smell Identification Test Score at 6 WeeksNasal Theophylline4Standard Error 2units on a scale
Change From Baseline in Smell Threshold Test Score at 6 WeeksNasal Theophylline-1Standard Error 2change in score on the scale
Change From Baseline in Plasma Theophylline Level at 6 WeeksNasal Theophylline0Standard Deviation 0microgram/mL

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDNasal Theophylline7
Overall StudyCOMPLETEDNasal Theophylline7
Overall StudyNOT COMPLETEDNasal Theophylline0

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 mortalityNasal Theophylline07
Total, other adverse eventsNasal Theophylline07
Total, serious adverse eventsNasal Theophylline07

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
19359985BACKGROUNDPubMed
23165381BACKGROUNDPubMed

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/NCT02479451

GET https://conductscience.org/api/trials/v1/NCT02479451/registered