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Trial · NCT00194896

Preferred Treatment of Type 1.5 Diabetes

NCT00194896, Not applicable, Completed, University of Washington; results first posted 2011-08-10

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Preferred Treatment of Type 1.5 Diabetes. Trials, record NCT00194896. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00194896

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Trial

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

Title
Preferred Treatment of Type 1.5 Diabetes
NCT number
NCT00194896
Status
Completed
Phases
Not applicable
Enrollment
64 participants, actual
Lead sponsor
University of Washington
Conditions
Type 2 Diabetes Mellitus
Interventions
rosiglitazone, glyburide
First posted
2005-09-19
Last updated
2018-03-29
Results first posted
2011-08-10
Limitations and caveats
Small numbers based on high drop out of participants.

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryChanges in Beta Cell Function Assessed by Fasting and Stimulated C-peptide Measured at 36 Months.36 monthsChanges in beta cell function assessed by fasting and stimulated C-peptide measured at 36 months.
SecondaryPatients Positive for T Cell Responses to Islet Proteins at 36 Months.36 monthsNumber of participants positive for T cell reactivity to islet proteins at 36 months.

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChanges in Beta Cell Function Assessed by Fasting and Stimulated C-peptide Measured at 36 Months.36 monthsAnalysis per protocolng per mlMEAN
SECONDARYPatients Positive for T Cell Responses to Islet Proteins at 36 Months.36 monthsparticipantsNUMBER

Results by group12

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

OutcomeGroupCategoryValueSpreadUnits
Changes in Beta Cell Function Assessed by Fasting and Stimulated C-peptide Measured at 36 Months.Rosiglitazone Autoantibody PositiveFasting C-peptide-0.4Standard Deviation 1.0ng per ml
Changes in Beta Cell Function Assessed by Fasting and Stimulated C-peptide Measured at 36 Months.Rosiglitazone Autoantibody NegativeFasting C-peptide-1.4Standard Deviation 1.6ng per ml
Changes in Beta Cell Function Assessed by Fasting and Stimulated C-peptide Measured at 36 Months.Glyburide Autoantibody PositiveFasting C-peptide0.1Standard Deviation 1.2ng per ml
Changes in Beta Cell Function Assessed by Fasting and Stimulated C-peptide Measured at 36 Months.Glyburide Autoantibody NegativeFasting C-peptide0.3Standard Deviation 1.1ng per ml
Changes in Beta Cell Function Assessed by Fasting and Stimulated C-peptide Measured at 36 Months.Rosiglitazone Autoantibody PositiveGlucagon Stimulated C-peptide-0.6Standard Deviation 1.6ng per ml
Changes in Beta Cell Function Assessed by Fasting and Stimulated C-peptide Measured at 36 Months.Rosiglitazone Autoantibody NegativeGlucagon Stimulated C-peptide-2.8Standard Deviation 2.5ng per ml
Changes in Beta Cell Function Assessed by Fasting and Stimulated C-peptide Measured at 36 Months.Glyburide Autoantibody PositiveGlucagon Stimulated C-peptide3.1Standard Deviation 12.1ng per ml
Changes in Beta Cell Function Assessed by Fasting and Stimulated C-peptide Measured at 36 Months.Glyburide Autoantibody NegativeGlucagon Stimulated C-peptide0.3Standard Deviation 2.2ng per ml
Patients Positive for T Cell Responses to Islet Proteins at 36 Months.Rosiglitazone Autoantibody Positive10participants
Patients Positive for T Cell Responses to Islet Proteins at 36 Months.Rosiglitazone Autoantibody Negative20participants

Participant flow12

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDRosiglitazone Autoantibody Positive15
Overall StudySTARTEDRosiglitazone Autoantibody Negative15
Overall StudySTARTEDGlyburide Autoantibody Positive13
Overall StudySTARTEDGlyburide Autoantibody Negative21
Overall StudyCOMPLETEDRosiglitazone Autoantibody Positive4
Overall StudyCOMPLETEDRosiglitazone Autoantibody Negative10
Overall StudyCOMPLETEDGlyburide Autoantibody Positive7
Overall StudyCOMPLETEDGlyburide Autoantibody Negative9
Overall StudyNOT COMPLETEDRosiglitazone Autoantibody Positive11
Overall StudyNOT COMPLETEDRosiglitazone Autoantibody Negative5

Adverse events24

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherHypoglycemiaEndocrine disordersRosiglitazone Autoantibody Positive0150
otherHypoglycemiaEndocrine disordersRosiglitazone Autoantibody Negative0150
otherHypoglycemiaEndocrine disordersGlyburide Autoantibody Positive1131
otherHypoglycemiaEndocrine disordersGlyburide Autoantibody Negative1211
seriousDeathGeneral disordersRosiglitazone Autoantibody Positive1151
seriousDeathGeneral disordersRosiglitazone Autoantibody Negative0150
seriousDeathGeneral disordersGlyburide Autoantibody Positive0130
seriousDeathGeneral disordersGlyburide Autoantibody Negative0210
seriousCholecystitisEndocrine disordersRosiglitazone Autoantibody Positive0150
seriousCholecystitisEndocrine disordersRosiglitazone Autoantibody Negative1151

Adverse event totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityRosiglitazone Autoantibody Positive
Total, all-cause mortalityRosiglitazone Autoantibody Negative
Total, all-cause mortalityGlyburide Autoantibody Positive
Total, all-cause mortalityGlyburide Autoantibody Negative
Total, other adverse eventsRosiglitazone Autoantibody Positive015
Total, other adverse eventsRosiglitazone Autoantibody Negative015
Total, other adverse eventsGlyburide Autoantibody Positive113
Total, other adverse eventsGlyburide Autoantibody Negative121
Total, serious adverse eventsRosiglitazone Autoantibody Positive115
Total, serious adverse eventsRosiglitazone Autoantibody Negative215

Papers35

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
1516769BACKGROUNDPubMed
1607079BACKGROUNDPubMed
1991568BACKGROUNDPubMed
2197139BACKGROUNDPubMed
2202883BACKGROUNDPubMed
2653752BACKGROUNDPubMed
3072143BACKGROUNDPubMed
3275559BACKGROUNDPubMed
3297896BACKGROUNDPubMed
3510930BACKGROUNDPubMed

1 to 10 of 35

See all 35 papers

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/NCT00194896

GET https://conductscience.org/api/trials/v1/NCT00194896/events?page=2