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Trial · NCT00229658

Outcomes12

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYIncidence of Patient-Ascertained Severe Hypoglycemia (PASH) During the Adjustment Period0-3 monthsIntent-to-TreatIncidence (%)NUMBER
PRIMARYAnnual Event Rate of Patient-Ascertained Severe Hypoglycemia (PASH) During the Adjustment Period0-3 monthsIntent-to-TreatEvents per patient yearNUMBER
SECONDARYThe Incidence of Patient-Ascertained Severe Hypoglycemia (PASH) During the Steady State Period>3-6 monthsIntent-to-Treat, number analyzed includes patients still enrolled in the study during the steady-state period (3-6 months)Incidence (%)NUMBER
SECONDARYThe Annual Event Rate of Patient-Ascertained Severe Hypoglycemia (PASH) During the Steady State Period>3-6 monthsIntent-to-Treat, number analyzed includes patients still enrolled in the study during the steady-state period (3-6 months)Events per patient yearNUMBER
SECONDARYIncidence of Medically Assisted Severe Hypoglycemia (MASH) During the Adjustment Period0-3 monthsIntent-to-Treat.Incidence (%)NUMBER
SECONDARYThe Annual Event Rate of Medically Assisted Severe Hypoglycemia (MASH) During the Adjustment Period0-3 monthsIntent-to-TreatEvents per patient yearNUMBER
SECONDARYIncidence of Medically Assisted Severe Hypoglycemia (MASH) During the Steady State Period>3-6 monthsIntent-to-Treat, number analyzed includes patients still enrolled in the study during the steady-state period (3-6 months)Incidence (%)NUMBER
SECONDARYAnnual Event Rate of Medically Assisted Severe Hypoglycemia (MASH) During the Steady State Period>3-6 monthsIntent-to-Treat, number analyzed includes patients still enrolled in the study during the steady-state period (3-6 months)Events per patient yearNUMBER
SECONDARYChange in HbA1c From Baseline at Month 33 monthsIntent-to-Treat, patients who discontinue SYMLIN 7 or more days prior to a site visit are not included in the analysespercentMEAN
SECONDARYChange in HbA1c From Baseline at Month 66 monthsIntent-to-Treat, patients who discontinue SYMLIN 7 or more days prior to a site visit are not included in the analysespercentMEAN
SECONDARYChange in Body Weight From Baseline at Month 33 monthsIntent-to-Treat, patients who discontinue SYMLIN 7 or more days prior to a site visit are not included in the analyseskgMEAN
SECONDARYChange in Body Weight From Baseline at Month 66 monthsIntent-to-Treat, patients who discontinue SYMLIN 7 or more days prior to a site visit are not included in the analyseskgMEAN

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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.

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