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Trial · NCT03514420

Registered outcomes43

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

ListOutcomeTime frameDescription
PrimaryPercent Change From Baseline in Fasting Triglycerides Levels at End of the Treatment (Week 27)Baseline and End of the Treatment (Week 27)The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment.
SecondaryChange From Baseline in Area Under the Curve (AUC) of Plasma Glucose as Assessed by Mixed Meal Test (MMT) at End of the TreatmentBaseline and End of the Treatment (Week 27)Change from Baseline to Week 27 in the area under the curve (AUC) of Plasma Glucose was assessed.
SecondaryChange From Baseline in AUC of Serum Insulin as Assessed by MMT at End of the TreatmentBaseline and End of the Treatment (Week 27)Change from Baseline to Week 27 in the AUC of Serum Insulin was assessed.
SecondaryChange From Baseline in AUC of Serum C-peptide as Assessed by MMT at End of the TreatmentBaseline and End of the Treatment (Week 27)Change from Baseline to Week 27 in the AUC of Serum C-peptide was assessed.
SecondaryChange From Baseline in AUC of Free Fatty Acid (FFA) as Assessed by MMT at End of the TreatmentBaseline and End of the Treatment (Week 27)Change from Baseline to Week 27 in the AUC of FFA was assessed.
SecondaryChange From Baseline in AUC of Serum Ghrelin as Assessed by MMT at End of the TreatmentBaseline and End of the Treatment (Week 27)Change from Baseline to Week 27 in the AUC of Serum Ghrelin was assessed.
SecondaryChange From Baseline in AUC of Incretin Hormone (Gastric Inhibitory Polypeptide [GIP]) as Assessed by MMT at End of the TreatmentBaseline and End of the Treatment (Week 27)Change from Baseline to Week 27 in the AUC of Incretin Hormone: GIP was assessed.
SecondaryChange From Baseline in AUC of Incretin Hormone (Glucagon-like Peptide -1 [GLP-1]) as Assessed by MMT at End of the TreatmentBaseline and End of the Treatment (Week 27)Change from Baseline to Week 27 in the AUC of Incretin Hormone: GLP-1 was assessed.
SecondaryChange From Baseline in AUC of Peptide Tyrosine Tyrosine (PYY) as Assessed by MMT at End of the TreatmentBaseline and End of the Treatment (Week 27)Change from Baseline to Week 27 in the AUC of PYY was assessed.
SecondaryChange From Baseline in HDL-C at End of the TreatmentBaseline and End of the Treatment (Week 27)The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment.
SecondaryChange From Baseline in LDL-C at End of the TreatmentBaseline and End of the Treatment (Week 27)
The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment. LDL-C calculated using ultracentrifugation method.
SecondaryChange From Baseline in Total Cholesterol (TC) at End of the TreatmentBaseline and End of the Treatment (Week 27)The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment.
SecondaryChange From Baseline in VLDL-C at End of the TreatmentBaseline and End of the Treatment (Week 27)
The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment. VLDL-C was calculated using direct test method.
SecondaryChange From Baseline in Non-HDL-C at End of the TreatmentBaseline and End of the Treatment (Week 27)The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment.
SecondaryChange From Baseline in ApoB at End of the TreatmentBaseline and End of the Treatment (Week 27)The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment.
SecondaryChange From Baseline in ApoB-48 at End of the TreatmentBaseline and End of the Treatment (Week 27)The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment.
SecondaryChange From Baseline in Apolipoprotein B 100 (ApoB-100) at End of the TreatmentBaseline and End of the Treatment (Week 27)The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment.
SecondaryChange From Baseline in ApoA-1 at End of the TreatmentBaseline and End of the Treatment (Week 27)The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment.
SecondaryChange From Baseline in ApoC-III at End of the TreatmentBaseline and End of the Treatment (Week 27)The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment.
SecondaryChange From Baseline in ApoC-III: Chylomicron at End of the TreatmentBaseline and End of the Treatment (Week 27)The baseline was defined as the average of Day 1 pre-dose fasting assessment and the last fasting measurement prior to Day 1 pre-dose fasting assessment.

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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GET https://conductscience.org/api/trials/v1/NCT03514420/registered