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Trial · NCT02048215

Registered outcomes13

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

ListOutcomeTime frameDescription
PrimaryChange in resting energy expenditureBaseline and 1 monthResting energy expenditure is measured by indirect calorimetry
SecondaryBlood pressure monitoringBaseline and daily for 30 days (t.i.d.)
SecondaryElectrocardiograpic monitoringBaseline and at week 2,3,4
SecondaryCardiac ultrasound monitoringBaseline and at week 2,3,4Cardiac ultrasound measurement for assessing possible detrimental changes
SecondaryChanges in fasting glucoseBaseline and at one monthPatients are assessed by oral glucose tolerance test at baseline and following one month of treatment, with assessment of glucose, insulin, free-fatty acids and glycerol
SecondaryChanges in fasting insulinbaseline and one monthPatients are assessed by oral glucose tolerance test at baseline and following one month of treatment, with assessment of glucose, insulin, free-fatty acids and glycerol
SecondaryChanges in fasting free fatty acidsbaseline ans one monthPatients are assessed by oral glucose tolerance test at baseline and following one month of treatment, with assessment of glucose, insulin, free-fatty acids and glycerol
SecondaryChanges in fasting glycerolbaseine and one monthPatients are assessed by oral glucose tolerance test at baseline and following one month of treatment, with assessment of glucose, insulin, free-fatty acids and glycerol
SecondaryChanges in thyroid function (TSH, T3, T4)Baseline and 1 month
SecondaryChanges in plasma noradrenalinBaseline and 1 month
SecondaryChanges in body weightbaseline and 1 month
SecondaryBeta-3 adrenoceptor expression in human adipose tissueone monthBeta-3 adrenoceptor expression is measured in subcutaneous and omental tissue sampled during bariatric surgery following one month of pharmacological intervention
SecondaryUCP-3 expression in human muscle tissueOne monthUCP-3 expression is measured in rectus abdominis muscle tissue sampled during bariatric surgery following one month of pharmacological intervention

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/NCT02048215/registered