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Study · Randomized controlled trial · n = 18 · 2003

6 results

Octreotide therapy of pediatric hypothalamic obesity: a double-blind, placebo-controlled trial.

Lustig RH, Hinds PS, Ringwald-Smith K, Christensen RK, Kaste SC, Schreiber RE, Rai SN, Lensing SY, Wu S, Xiong X

The Journal of clinical endocrinology and metabolism1 Jun 2003Cited by 181 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study6

6 results from studies that gave the peptide. 6 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In children with hypothalamic obesity, weight increased by 1.6 +/- 0.6 kg with octreotide versus 9.1 +/- 1.7 kg with placebo (P < 0.001).

    In plain wordsIn children with hypothalamic obesity, octreotide reduced weight gain compared with placebo.

    Peptide
    Octreotide
    Outcome
    DecreaseWeight change
    Study

    n = 18

    Comparator
    Placebo
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    5-15 microg/kg per day · subcutaneous · 6 monthsAs given in this study (human).

    Measurements

    Weight change, mean
    1.6 kg
    octreotide group; SEM 0.6
    Weight change, mean
    9.1 kg
    placebo group; SEM 1.7

    Source sentences

    Summary
    With octreotide, Delta weight (mean +/- SEM) was +1.6 +/- 0.6 vs. +9.1 +/- 1.7 kg for placebo (P < 0.001).
    2 context sentences
    Summary · context
    We report the results of a randomized, double-blind, placebo-controlled trial of octreotide therapy for pediatric hypothalamic obesity.
    Summary · context
    Eighteen subjects [weight, 100.6 +/- 5.6 kg; body mass index (BMI), 37.1 +/- 1.3 kg/m(2)] received octreotide (5-15 microg/kg x d s.c.) or placebo for 6 months.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In children with hypothalamic obesity, BMI changed by -0.2 +/- 0.2 versus +2.2 +/- 0.5 kg/m(2) with placebo (P < 0.001).

    In plain wordsIn children with hypothalamic obesity, octreotide reduced BMI change compared with placebo.

    Peptide
    Octreotide
    Outcome
    DecreaseBMI change
    Study

    n = 18

    Comparator
    Placebo
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    5-15 microg/kg per day · subcutaneous · 6 monthsAs given in this study (human).

    Measurements

    BMI change, mean
    −0.2 kg/m(2)
    octreotide group; SEM 0.2
    BMI change, mean
    2.2 kg/m(2)
    placebo group; SEM 0.5

    Source sentences

    Summary
    Delta BMI was -0.2 +/- 0.2 vs. +2.2 +/- 0.5 kg/m(2), respectively (P < 0.001).
    3 context sentences
    Summary · context
    With octreotide, Delta weight (mean +/- SEM) was +1.6 +/- 0.6 vs. +9.1 +/- 1.7 kg for placebo (P < 0.001).
    Summary · context
    We report the results of a randomized, double-blind, placebo-controlled trial of octreotide therapy for pediatric hypothalamic obesity.
    Summary · context
    Eighteen subjects [weight, 100.6 +/- 5.6 kg; body mass index (BMI), 37.1 +/- 1.3 kg/m(2)] received octreotide (5-15 microg/kg x d s.c.) or placebo for 6 months.
  3. 03HumanRandomized controlled trialEfficacy outcome

    In children with hypothalamic obesity, insulin response changed by -417 +/- 304 pM with octreotide versus +216 +/- 215 with placebo (P = 0.034).

    In plain wordsIn children with hypothalamic obesity, octreotide reduced the insulin response to glucose compared with placebo.

    Peptide
    Octreotide
    Outcome
    DecreaseOGTT insulin response change
    Study

    n = 18

    Comparator
    Placebo
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5-15 microg/kg per day · subcutaneous · 6 monthsAs given in this study (human).

    Measurements

    Delta insulin response (peak - basal), mean
    −417 pM
    octreotide group; SEM 304
    Delta insulin response (peak - basal), mean
    216 pM
    placebo group; SEM 215

    Source sentences

    Summary
    OGTT documented Delta insulin response (peak - basal) of -417 +/- 304 pM after octreotide vs. +216 +/- 215 pM after placebo (P = 0.034).
    2 context sentences
    Summary · context
    We report the results of a randomized, double-blind, placebo-controlled trial of octreotide therapy for pediatric hypothalamic obesity.
    Summary · context
    Eighteen subjects [weight, 100.6 +/- 5.6 kg; body mass index (BMI), 37.1 +/- 1.3 kg/m(2)] received octreotide (5-15 microg/kg x d s.c.) or placebo for 6 months.
  4. 04HumanRandomized controlled trialEfficacy outcome

    In children with hypothalamic obesity, parent-reported physical activity improved with octreotide but not placebo (P = 0.03).

    In plain wordsIn children with hypothalamic obesity, parents reported improved activity with octreotide but not placebo.

    Peptide
    Octreotide
    Outcome
    Direction not reportedParent-reported physical activity
    Study

    n = 18

    Comparator
    Placebo
    Outcome group
    Exercise and physical function · Metabolic and weight
    Studied dose
    5-15 microg/kg per day · subcutaneous · 6 monthsAs given in this study (human).

    Source sentences

    Summary
    Improvement in physical activity by parent report was noted with octreotide, but not placebo (P = 0.03).
    2 context sentences
    Summary · context
    We report the results of a randomized, double-blind, placebo-controlled trial of octreotide therapy for pediatric hypothalamic obesity.
    Summary · context
    Eighteen subjects [weight, 100.6 +/- 5.6 kg; body mass index (BMI), 37.1 +/- 1.3 kg/m(2)] received octreotide (5-15 microg/kg x d s.c.) or placebo for 6 months.
  5. 05HumanNon-randomized trialSafety outcome

    In children treated for hypothalamic obesity, complications and adverse events were mild and self-limited.

    In plain wordsIn children treated for hypothalamic obesity, complications and side effects were mild and self-limited.

    Peptide
    Octreotide
    Outcome
    Not applicableComplications and adverse event severity
    Study

    n: not reported in source

    Outcome group
    Adverse events · Whole body
    Studied dose
    5-15 microg/kg per day · subcutaneous · 6 monthsAs given in this study (human).

    Source sentences

    Summary
    Complications and adverse events were mild and self-limited.
    2 context sentences
    Summary · context
    We report the results of a randomized, double-blind, placebo-controlled trial of octreotide therapy for pediatric hypothalamic obesity.
    Summary · context
    Eighteen subjects [weight, 100.6 +/- 5.6 kg; body mass index (BMI), 37.1 +/- 1.3 kg/m(2)] received octreotide (5-15 microg/kg x d s.c.) or placebo for 6 months.
  6. 06HumanObservational studyEfficacy outcome

    In children receiving octreotide for hypothalamic obesity, quality-of-life changes correlated positively with insulin-response changes (P = 0.041).

    In plain wordsIn children receiving octreotide, quality-of-life changes were positively linked to insulin-response changes.

    Peptide
    Octreotide
    Outcome
    Not applicableQuality of life correlation with insulin response
    Study

    n: not reported in source

    Outcome group
    Quality of life · Whole body
    Studied dose
    5-15 microg/kg per day · subcutaneous · 6 monthsAs given in this study (human).

    Source sentences

    Summary
    For the octreotide group, changes in quality of life positively correlated with changes in insulin response (P = 0.041).
    2 context sentences
    Summary · context
    We report the results of a randomized, double-blind, placebo-controlled trial of octreotide therapy for pediatric hypothalamic obesity.
    Summary · context
    Eighteen subjects [weight, 100.6 +/- 5.6 kg; body mass index (BMI), 37.1 +/- 1.3 kg/m(2)] received octreotide (5-15 microg/kg x d s.c.) or placebo for 6 months.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    28 Oct 2026, 02:03 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:36 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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