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Trial · NCT03548935

Outcomes42

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Body Weight (%)Baseline (week 0) to week 68Overall number of participants analyzed = full analysis set (FAS) which comprised all randomized participants. Number Analyzed = number of participants with available data.Percentage pointMEAN
PRIMARYParticipants Who Achieve 5 or More Percent Body Weight Reduction (Yes/no)After week 68Overall number of participants analyzed = full analysis set (FAS) which comprised all randomized participants. Number Analyzed = number of participants with available data.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYSubjects Who Achieve 10 or More Percent Body Weight Reduction (Yes/no)Week 68FAS included all randomized participants. 'Overall Number of Participants Analyzed' = participants with available data.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYParticipants Who Achieve 15 or More Percent Body Weight Reduction (Yes/no)Week 68FAS included all randomised participants. 'Overall Number of Participants Analyzed' = participants with available data.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYParticipants Who Achieve 20 or More Percent Body Weight Reduction (Yes/no)Week 68FAS included all randomised participants. 'Overall Number of Participants Analyzed' = participants with available data.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYChange in Waist Circumference (cm)Baseline (week 0) to week 68FAS included all randomised participants. 'Overall Number of Participants Analyzed' = participants with available data.Centimeter (cm)MEAN
SECONDARYChange in Systolic Blood Pressure (mmHg)Baseline (week 0) to week 68FAS included all randomised participants. 'Overall Number of Participants Analyzed' = participants with available data.Millimeters of mercury (mmHg)MEAN
SECONDARYChange in Short Form 36 (SF-36)Baseline (week 0) to week 68FAS included all randomised participants. 'Overall Number of Participants Analyzed' = participants with available data.Score on a scaleMEAN
SECONDARYChange in Impact of Weight on Quality of Life-Lite for Clinical Trial (IWQoL-Lite for CT) ScoreBaseline (week 0) to week 68FAS included all randomized participants. 'Overall Number of Participants Analyzed' = participants with available data.Score on a scaleMEAN
SECONDARYChange in Body Weight (kg)Baseline (week 0) to week 68FAS included all randomized participants. 'Overall Number of Participants Analyzed' = participants with available data.Kilogram (kg)MEAN
SECONDARYChange in Body Mass Index (BMI) (kg/m2)Baseline (week 0) to week 68Overall number of participants analyzed = full analysis set (FAS) which comprised all randomized participants. Number Analyzed = number of participants with available data.Kilogram per square meter (kg/sqm)MEAN
SECONDARYChange in HbA1C (%)Baseline (week 0) to week 68FAS included all randomized participants. 'Overall Number of Participants Analyzed' = participants with available data.Percentage point of HbA1cMEAN
SECONDARYChange in HbA1C (mmol/Mol)Baseline (week 0) to week 68FAS included all randomized participants. 'Overall Number of Participants Analyzed' = participants with available data.millimoles per mole (mmol/mol)MEAN
SECONDARYChange in Fasting Plasma Glucose (FPG) (mg/dL)Baseline (week 0) to week 68FAS included all randomized participants. 'Overall Number of Participants Analyzed' = participants with available data.milligrams per deciliter (mg/dL)MEAN
SECONDARYChange in Fasting Serum Insulin (mIU/L) - Ratio to BaselineBaseline (week 0) to week 68FAS included all randomised participants. 'Overall Number of Participants Analyzed' = participants with available data.Ratio of fasting serum insulinGEOMETRIC_MEAN
SECONDARYChange in Diastolic Blood Pressure (mmHg)Baseline (week 0) to week 68FAS included all randomized participants. 'Overall Number of Participants Analyzed' = participants with available data.Millimeters of mercury (mmHg)MEAN
SECONDARYChange in Total Cholesterol (mg/dL) - Ratio to BaselineBaseline (week 0) to week 68FAS included all randomised participants. 'Overall Number of Participants Analyzed' = participants with available data.Ratio of total cholesterolGEOMETRIC_MEAN
SECONDARYChange in High-density Lipoproteins (HDL) (mg/dL) - Ratio to BaselineBaseline (week 0) to week 68FAS included all randomised participants. 'Overall Number of Participants Analyzed' = participants with available data.Ratio of HDL cholesterolGEOMETRIC_MEAN
SECONDARYChange in Low-density Lipoproteins (LDL) (mg/dL) - Ratio to BaselineBaseline (week 0) to week 68FAS included all randomised participants. 'Overall Number of Participants Analyzed' = participants with available data.Ratio of LDL cholesterolGEOMETRIC_MEAN
SECONDARYChange in Very Low-density Lipoproteins (VLDL) (mg/dL) - Ratio to BaselineBaseline (week 0) to week 68FAS included all randomised participants. 'Overall Number of Participants Analyzed' = participants with available data.Ratio of VLDL cholesterolGEOMETRIC_MEAN

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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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT03548935/outcomes