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Trial · NCT00752726

Outcomes11

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline to Week 24 in Abdominal VAT MassBaseline to week 24This analysis was carried out for the observed ITT population, who had this post-baseline efficacy assessment.kgMEAN
SECONDARYChange From Baseline to Week 12 in Abdominal VAT MassBaseline to week 12This analysis was carried out for the observed ITT population, who had this post-baseline efficacy assessment.kgMEAN
SECONDARYChange From Baseline to Week 24 in Body WeightBaseline to week 24This analysis was carried out for the observed ITT population, who had this post-baseline efficacy assessment.kgMEAN
SECONDARYChange From Baseline to Week 24 in Total Fat MassBaseline to week 24This analysis was carried out for the observed ITT population, who had this post-baseline efficacy assessment.kgMEAN
SECONDARYChange From Baseline to Week 24 in Percentage Body FatBaseline to week 24This analysis was carried out for the observed ITT population, who had this post-baseline efficacy assessment.Percentage (%) body fatMEAN
SECONDARYChange From Baseline to Week 24 in Waist CircumferenceBaseline to week 24This analysis was carried out for the observed ITT population, who had this post-baseline efficacy assessment.cmMEAN
SECONDARYChange From Baseline to Week 24 in Percentage Liver FatBaseline to week 24ITT subset (participants who had this post-baseline efficacy assessment) from one study site was analysed for this parameter.Percentage (%) IHLMEAN
SECONDARYChange From Baseline to Week 24 in Liver FatBaseline to week 24This analysis was carried out for the observed ITT population, who had this post-baseline efficacy assessment.Hounsfield Units (HU)MEAN
SECONDARYChange From Baseline to Week 24 in Total Calories Expended for Physical ActivityBaseline to week 24This analysis was carried out for the observed ITT population, who had this post-baseline efficacy assessment.Kilocalorie (kcal)/weekMEAN
SECONDARYChange From Baseline to Week 24 in Quality of Life (QoL) Scores.Baseline to week 24This analysis was carried out for the observed ITT population, i.e. ITT subjects who had this post-baseline efficacy assessment.Score on a ScaleMEAN
SECONDARYSelectivity Index at Week 24Baseline to week 24This analysis was carried out for the observed ITT population, who had this post-baseline efficacy assessment, only in Orlistat 60 mg group. This analysis was not carried out for placebo group.RatioNUMBER

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/NCT00752726/outcomes