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Trial · NCT00422058

Outcomes20

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMean Change From Baseline in Body Weight at Week 20Week 0, week 20
ITT (intention to treat) analysis set using LOCF (last observation carried forward) is all randomised and exposed subjects from the double-blind period, who have been exposed to at least one dose of trial product.
kgMEAN
SECONDARYMean Change From Baseline in Body Weight at Week 104Week 0, week 104
ITT (intention to treat) analysis set using LOCF (last observation carried forward) is all randomised and exposed subjects from the double-blind period, who have been exposed to at least one dose of trial product.
kgMEAN
SECONDARYChange From Baseline in Fasting Plasma Glucose at Week 20Week 0, week 20
ITT (intention to treat) analysis set using (LOCF) last observation carried forward is all randomised and exposed subjects from the double-blind period, who have been exposed to at least one dose of trial product
mmol/LMEAN
SECONDARYChange From Baseline in Fasting Plasma Glucose at Week 104Week 0, week 104
ITT (intention to treat) analysis set using (LOCF) last observation carried forward is all randomised and exposed subjects from the double-blind period, who have been exposed to at least one dose of trial product
mmol/LMEAN
SECONDARYChange From Baseline in Fasting Insulin at Week 20Week 0, week 20ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).pmol/LMEAN
SECONDARYChange From Baseline in Fasting Insulin at Week 104Week 0, week 104ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).pmol/LMEAN
SECONDARYChange From Baseline in HbA1c (Glycosylated Haemoglobin A1c) at Week 20Week 0, week 20ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).percentage (%) of total haemoglobinMEAN
SECONDARYChange From Baseline in HbA1c (Glycosylated Haemoglobin A1c) at Week 104Week 0, week 104ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).percentage (%) of total haemoglobinMEAN
SECONDARYChange From Baseline in hsCRP (Highly Sensitive C-reactive Protein) at Week 20Week 0, week 20ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).mg/LMEAN
SECONDARYChange From Baseline in hsCRP (Highly Sensitive C-reactive Protein) at Week 104Week 0, week 104ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).mg/LMEAN
SECONDARYChange From Baseline in PAI-1 (Plasminogen Activator Inhibitor 1) at Week 20Week 0, week 20ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).U/mLMEAN
SECONDARYChange From Baseline in PAI-1 (Plasminogen Activator Inhibitor 1) at Week 104Week 0, week 104ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).U/mLMEAN
SECONDARYChange From Baseline in Fibrinogen at Week 20Week 0, week 20ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).g/LMEAN
SECONDARYChange From Baseline in Fibrinogen at Week 104Week 0, week 104ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).g/LMEAN
SECONDARYChange From Baseline in Adiponectin at Week 20Week 0, week 20ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).mcg/mLMEAN
SECONDARYChange From Baseline in Adiponectin at Week 104Week 0, week 104ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).mcg/mLMEAN
SECONDARYChange From Baseline in Waist Circumference at Week 20Week 0, week 20ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).cmMEAN
SECONDARYChange From Baseline in Waist Circumference at Week 104Week 0, week 104ITT (intention to treat) analysis set, only subjects with a valid assessment (LOCF, last observation carried forward not applied).cmMEAN
SECONDARYChange From Baseline in Blood Pressure at Week 20Week 0, week 20
ITT (intention to treat) analysis set using (LOCF) last observation carried forward is all randomised and exposed subjects from the double-blind period, who have been exposed to at least one dose of trial product
mmHgMEAN
SECONDARYChange From Baseline in Blood Pressure at Week 104Week 0, week 104
ITT (intention to treat) analysis set using (LOCF) last observation carried forward is all randomised and exposed subjects from the double-blind period, who have been exposed to at least one dose of trial product
mmHgMEAN

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.

For software

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GET https://conductscience.org/api/trials/v1/NCT00422058/outcomes