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Study · Non-randomized trial · n = 20 · 2006

6 results

Treatment of central precocious puberty with triptorelin 11.25 mg depot formulation.

Martínez-Aguayo A, Hernández MI, Beas F, Iñiguez G, Avila A, Sovino H, Bravo E, Cassorla F

Journal of pediatric endocrinology & metabolism : JPEM1 Aug 2006Cited by 19 (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. 01HumanNon-randomized trialEfficacy outcome

    In children with central precocious puberty, triptorelin significantly reduced basal LH from baseline to 3 months.

    In plain wordsIn children with central precocious puberty, triptorelin reduced basal LH compared with baseline after 3 months.

    Outcome
    DecreaseBasal LH
    Study

    n = 20

    Comparator
    Baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    11.25 mg every 90 days · 3 monthsAs given in this study (human).

    Source sentences

    Summary
    The basal and GnRH-stimulated serum levels of LH and FSH decreased significantly from baseline to 3 months of therapy (p <0.0001).
    2 context sentences
    Summary · context
    The aim of our study was to evaluate the efficacy of triptorelin 11.25 mg administered every 90 days to suppress gonadotropin and sex steroid secretion and pubertal signs in children with CPP during 2 years of treatment.
    Summary · context
    We studied 20 patients (19 girls and 1 boy), with a median age at entry into the study of 7.5 +/- 0.2 years for girls, and 9 years for the boy.
  2. 02HumanNon-randomized trialEfficacy outcome

    In children with central precocious puberty, triptorelin significantly reduced GnRH-stimulated LH from baseline to 3 months.

    In plain wordsIn children with central precocious puberty, triptorelin reduced stimulated LH compared with baseline after 3 months.

    Outcome
    DecreaseGnRH-stimulated LH
    Study

    n = 20

    Comparator
    Baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    11.25 mg every 90 days · 3 monthsAs given in this study (human).

    Source sentences

    Summary
    The basal and GnRH-stimulated serum levels of LH and FSH decreased significantly from baseline to 3 months of therapy (p <0.0001).
    2 context sentences
    Summary · context
    The aim of our study was to evaluate the efficacy of triptorelin 11.25 mg administered every 90 days to suppress gonadotropin and sex steroid secretion and pubertal signs in children with CPP during 2 years of treatment.
    Summary · context
    We studied 20 patients (19 girls and 1 boy), with a median age at entry into the study of 7.5 +/- 0.2 years for girls, and 9 years for the boy.
  3. 03HumanNon-randomized trialEfficacy outcome

    In children with central precocious puberty, triptorelin significantly reduced basal FSH from baseline to 3 months.

    In plain wordsIn children with central precocious puberty, triptorelin reduced basal FSH compared with baseline after 3 months.

    Outcome
    DecreaseBasal FSH
    Study

    n = 20

    Comparator
    Baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    11.25 mg every 90 days · 3 monthsAs given in this study (human).

    Source sentences

    Summary
    The basal and GnRH-stimulated serum levels of LH and FSH decreased significantly from baseline to 3 months of therapy (p <0.0001).
    2 context sentences
    Summary · context
    The aim of our study was to evaluate the efficacy of triptorelin 11.25 mg administered every 90 days to suppress gonadotropin and sex steroid secretion and pubertal signs in children with CPP during 2 years of treatment.
    Summary · context
    We studied 20 patients (19 girls and 1 boy), with a median age at entry into the study of 7.5 +/- 0.2 years for girls, and 9 years for the boy.
  4. 04HumanNon-randomized trialEfficacy outcome

    In children with central precocious puberty, triptorelin significantly reduced GnRH-stimulated FSH from baseline to 3 months.

    In plain wordsIn children with central precocious puberty, triptorelin reduced stimulated FSH compared with baseline after 3 months.

    Outcome
    DecreaseGnRH-stimulated FSH
    Study

    n = 20

    Comparator
    Baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    11.25 mg every 90 days · 3 monthsAs given in this study (human).

    Source sentences

    Summary
    The basal and GnRH-stimulated serum levels of LH and FSH decreased significantly from baseline to 3 months of therapy (p <0.0001).
    2 context sentences
    Summary · context
    The aim of our study was to evaluate the efficacy of triptorelin 11.25 mg administered every 90 days to suppress gonadotropin and sex steroid secretion and pubertal signs in children with CPP during 2 years of treatment.
    Summary · context
    We studied 20 patients (19 girls and 1 boy), with a median age at entry into the study of 7.5 +/- 0.2 years for girls, and 9 years for the boy.
  5. 05HumanNon-randomized trialEfficacy outcome

    In children with central precocious puberty receiving triptorelin, all patients had a GnRH-stimulated peak below 3 mIU/ml between 6 and 24 months.

    In plain wordsIn children receiving triptorelin for precocious puberty, all stimulated peaks stayed below 3 mIU/ml between 6 and 24 months.

    Outcome
    DecreaseGnRH-stimulated peak suppression
    Study

    n = 20

    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    11.25 mg every 90 days · 6 to 24 monthsAs given in this study (human).

    Measurements

    GnRH-stimulated peak
    < 3 mIU/ml
    all patients between 6 and 24 months

    Source sentences

    Summary
    All patients had a GnRH-stimulated peak below 3 mIU/ml between 6 and 24 months of treatment.
    2 context sentences
    Summary · context
    The aim of our study was to evaluate the efficacy of triptorelin 11.25 mg administered every 90 days to suppress gonadotropin and sex steroid secretion and pubertal signs in children with CPP during 2 years of treatment.
    Summary · context
    We studied 20 patients (19 girls and 1 boy), with a median age at entry into the study of 7.5 +/- 0.2 years for girls, and 9 years for the boy.
  6. 06HumanNon-randomized trialEfficacy outcome

    In children treated with triptorelin for central precocious puberty, the pituitary-gonadal axis recovered adequately after treatment stopped.

    In plain wordsIn children treated with triptorelin for precocious puberty, the pituitary-gonadal axis recovered after treatment stopped.

    Outcome
    Not applicablePituitary-gonadal axis recovery
    Study

    n = 20

    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    11.25 mg every 90 days · 2 yearsAs given in this study (human).

    Source sentences

    Summary
    The pituitary-gonadal axis recovered adequately after discontinuation of therapy.
    2 context sentences
    Summary · context
    The aim of our study was to evaluate the efficacy of triptorelin 11.25 mg administered every 90 days to suppress gonadotropin and sex steroid secretion and pubertal signs in children with CPP during 2 years of treatment.
    Summary · context
    We studied 20 patients (19 girls and 1 boy), with a median age at entry into the study of 7.5 +/- 0.2 years for girls, and 9 years for the boy.

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

Registered trials1

Trials this study reports on, or that list this study as a reference. Registry data from ClinicalTrials.gov.

1 trial · 1 completed · 1 with posted results · source ClinicalTrials.gov (opens in a new tab)

CompletedPhase 3Results postedNCT01467882

Efficacy, Safety, and Pharmacokinetics (PK) of Triptorelin 6-month Formulation in Patients With Central Precocious Puberty

Debiopharm International SAn = 44Apr 2012 to Jul 2014

Central Precocious Puberty

Trial pageClinicalTrials.govUpdated 28 Jul 2017

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

    22 Oct 2026, 02:26 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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