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Trial · NCT00399893

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryNumber of Participants With Decrease in Fasting Total Ghrelin6 monthsNumber of participants showing a decrease in Fasting total ghrelin from baseline to 6 months of treatment with Octreotide or placebo
PrimaryNumber of Participants With Decrease in Weight From Baseline to 6 Months6 monthsNumber of participants who had a decrease in weight from baseline to 6 months of Octreotide or placebo therapy
PrimaryNumber of Participants With Decreased BMI Z-score From Baseline to 6 Months6 monthsNumber of participants with decreased BMI z-score from baseline to 6 months of Octreotide or Placebo therapy
PrimaryNumber of Participants With Decreased Skin-fold Measurements From Baseline to 6 Months6 monthsNumber of participants with decreased skin-fold measurements from baseline to 6 months of Octreotide or Placebo therapy
PrimaryNumber of Participants With Decrease in Hunger and Food Intake6 months
Measured by hunger and hyperphagia by questionnaires and parent-reported 72-hour food recall from baseline to 6 months. Multiple questionnaires consisting of a battery of free text answer questions and food diaries are combined in order to make a behavioral assessment of the participants food state of hunger and food intake. There is no defined scale for this assessment. Each participants responses and parent responses are combined.
PrimaryNumber of Participants With Improved Insulin Regulation From Baseline to 6 Months6 monthsNumber of participants with improved Insulin regulation from baseline to 6 months of Octreotide or Placebo therapy. Insulin regulation was measured by immunochemiluminescent assay.
PrimaryNumber of Participants With Improved Adiponectin Regulation From Baseline to 6 Months6 monthsNumber of participants with improved Adiponectin regulation from baseline to 6 months of Octreotide or Placebo therapy
PrimaryNumber of Participants With Improved Leptin Regulation From Baseline to 6 Months6 monthsNumber of participants with improved Leptin regulation from baseline to 6 months of Octreotide or Placebo therapy
PrimaryNumber of Participants With Improved Peptide YY (PYY) Regulation From Baseline to 6 Months6 monthsNumber of participants with improved Peptide YY (PYY) regulation from baseline to 6 months of Octreotide or Placebo therapy
SecondaryNumber of Participants With Decreased Body Composition From Baseline to 6 Months by BOD POD®6 monthsNumber of participants with decreased body-composition as Measured by BOD POD® body composition tracking system from baseline to 6 months of Octreotide or Placebo therapy
SecondaryNumber of Participants With Decreased Body-composition From Baseline to 6 Months by DEXA6 monthsNumber of participants with decreased body-composition as Measured by Dual Energy X-ray Absorptiometry (DEXA) scan from baseline to 6 months of Octreotide or Placebo therapy

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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