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Trial · NCT06323174

Registered outcomes31

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

ListOutcomeTime frameDescription
PrimaryChange in glycated haemoglobin (HbA1c)From baseline (week 0) to end of treatment (week 40)Measured as percentage (%)-points.
SecondaryRelative change in body weightFrom baseline (week 0) to end of treatment (week 40)Measured in %.
SecondaryNumber of participants who achieve greater than or equal to (>=) 10% body weight reductionFrom baseline (week 0) to end of treatment (week 40)Measured as count of participants.
SecondaryNumber of participants who achieve >=15% body weight reductionFrom baseline (week 0) to end of treatment (week 40)Measured as count of participants.
SecondaryNumber of participants who achieve HbA1c target values of less than (<) 7.0% (<53 millimoles per mole [mmol/mol])At end of treatment (week 40)Measured as count of participants.
SecondaryNumber of participants who achieve HbA1c target values of less than or equal to (<=) 6.5% (<= 48 mmol/mol)At end of treatment (week 40)Measured as count of participants.
SecondaryChange in Fasting Plasma Glucose (FPG)From baseline (week 0) to end of treatment (week 40)Measured in millimoles per liter (mmol/L).
SecondaryNumber of participants who achieve >=5% body weight reductionFrom baseline (week 0) to end of treatment (week 40)Measured as count of participants.
SecondaryNumber of participants who achieve >=20% body weight reductionFrom baseline (week 0) to end of treatment (week 40)Measured as count of participants.
SecondaryChange in waist circumferenceFrom baseline (week 0) to end of treatment (week 40)Measured in centimeters (cm).
SecondaryChange in systolic blood pressure (SBP)From baseline (week 0) to end of treatment (week 40)Measured in millimeters of mercury (mmHg).
SecondaryChange in diastolic blood pressure (DBP)From baseline (week 0) to end of treatment (week 40)Measured in mmHg.
SecondaryRatio to baseline in high sensitivity C-reactive protein (hsCRP)From baseline (week 0) to end of treatment (week 40)Measured as ratio.
SecondaryRatio to baseline in lipids: Total cholesterolFrom baseline (week 0) to end of treatment (week 40)Measured as ratio.
SecondaryRatio to baseline in lipids: High-density lipoprotein (HDL) cholesterolFrom baseline (week 0) to end of treatment (week 40)Measured as ratio.
SecondaryRatio to baseline in lipids: Low-density lipoprotein (LDL) cholesterolFrom baseline (week 0) to end of treatment (week 40)Measured as ratio.
SecondaryRatio to baseline in lipids: Very low-density lipoprotein (VLDL) cholesterolFrom baseline (week 0) to end of treatment (week 40)Measured as ratio.
SecondaryRatio to baseline in lipids: TriglyceridesFrom baseline (week 0) to end of treatment (week 40)Measured as ratio.
SecondaryRatio to baseline in lipids: Free fatty acidsFrom baseline (week 0) to end of treatment (week 40)Measured as ratio.
SecondaryRatio to baseline in lipids: Non-HDL cholesterolFrom baseline (week 0) to end of treatment (week 40)Measured as ratio.

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/NCT06323174/registered