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Study · Randomized controlled trial · n = 205 · 2004

3 results

The effect of an individualized GnRH antagonist protocol on folliculogenesis in IVF/ICSI.

Mochtar MH

Human reproduction (Oxford, England)30 Jun 2004Cited by 44 (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 study3

3 results from studies that gave the peptide. 3 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In IVF/ICSI patients, retrieved oocytes did not differ significantly between flexible ganirelix (9.4, SD 5.8) and fixed ganirelix (9.7, SD 6.5).

    In plain wordsIn IVF/ICSI patients, retrieved oocytes did not differ significantly between flexible ganirelix and fixed ganirelix.

    Peptide
    Ganirelix
    Outcome
    No significant changeRetrieved oocytes
    Study

    n = 205

    Comparator
    fixed ganirelix regimen starting on stimulation day 6
    Analysis
    Primary
    Outcome group
    Sex hormones and fertility · Reproductive and sexual health
    Studied dose
    0.25 mg dailyAs given in this study (human).

    Measurements

    Mean retrieved oocytes
    9.4 oocytes
    flexible regimen
    SD of retrieved oocytes
    5.8 oocytes
    flexible regimen
    Mean retrieved oocytes
    9.7 oocytes
    fixed regimen
    SD of retrieved oocytes
    6.5 oocytes
    fixed regimen

    Source sentences

    Summary
    The mean (SD) number of retrieved oocytes was not statistically significantly different: 9.4 (5.8) in the flexible group versus 9.7 (6.5) in the fixed group.
    2 context sentences
    Summary · context
    In a multicentre, randomized, clinical trial, IVF/ICSI patients were allocated to a standard regimen, in which they received daily 0.25 mg GnRH antagonist ganirelix (Orgalutran) from the 6th day of stimulation onward (fixed regimen n = 102)
    Summary · context
    or to an individualized regimen, in which IVF/ICSI patients received daily 0.25 mg GnRH antagonist starting on the day that the dominant follicle had reached a diameter of > or = 15 mm (flexible regimen n = 103).
  2. 02HumanRandomized controlled trialEfficacy outcome

    In IVF/ICSI patients, clinical pregnancy rates were 22.7% with flexible ganirelix versus 33% with fixed ganirelix, relative rate ratio 0.69 (95% CI 0.44-1.08).

    In plain wordsIn IVF/ICSI patients, clinical pregnancy rates were 22.7% with flexible ganirelix versus 33% with fixed ganirelix.

    Peptide
    Ganirelix
    Outcome
    DecreaseClinical pregnancy rate
    Study

    n = 205

    Comparator
    fixed ganirelix regimen starting on stimulation day 6
    Outcome group
    Sex hormones and fertility · Reproductive and sexual health
    Studied dose
    0.25 mg dailyAs given in this study (human).

    Measurements

    Clinical pregnancy rate
    22.7%
    flexible regimen
    Clinical pregnancy rate
    33%
    fixed regimen
    Relative rate ratio
    0.69 ratio
    flexible versus fixed
    95% confidence interval of relative rate ratio
    0.44 to 1.08 ratio
    flexible versus fixed

    Source sentences

    Summary
    The clinical and ongoing pregnancy rates were 22.7 and 21.8% respectively in the flexible group versus 33 and 31.1% in the fixed group [relative rate ratio 0.69 (95% confidence interval 0.44-1.08) and 0.7 (0.44-1.12) respectively].
    2 context sentences
    Summary · context
    In a multicentre, randomized, clinical trial, IVF/ICSI patients were allocated to a standard regimen, in which they received daily 0.25 mg GnRH antagonist ganirelix (Orgalutran) from the 6th day of stimulation onward (fixed regimen n = 102)
    Summary · context
    or to an individualized regimen, in which IVF/ICSI patients received daily 0.25 mg GnRH antagonist starting on the day that the dominant follicle had reached a diameter of > or = 15 mm (flexible regimen n = 103).
  3. 03HumanRandomized controlled trialEfficacy outcome

    In IVF/ICSI patients, ongoing pregnancy rates were 21.8% with flexible ganirelix versus 31.1% with fixed ganirelix, relative rate ratio 0.7 (0.44-1.12).

    In plain wordsIn IVF/ICSI patients, ongoing pregnancy rates were 21.8% with flexible ganirelix versus 31.1% with fixed ganirelix.

    Peptide
    Ganirelix
    Outcome
    DecreaseOngoing pregnancy rate
    Study

    n = 205

    Comparator
    fixed ganirelix regimen starting on stimulation day 6
    Outcome group
    Sex hormones and fertility · Reproductive and sexual health
    Studied dose
    0.25 mg dailyAs given in this study (human).

    Measurements

    Ongoing pregnancy rate
    21.8%
    flexible regimen
    Ongoing pregnancy rate
    31.1%
    fixed regimen
    Relative rate ratio
    0.7 ratio
    flexible versus fixed
    95% confidence interval of relative rate ratio
    0.44 to 1.12 ratio
    flexible versus fixed

    Source sentences

    Summary
    The clinical and ongoing pregnancy rates were 22.7 and 21.8% respectively in the flexible group versus 33 and 31.1% in the fixed group [relative rate ratio 0.69 (95% confidence interval 0.44-1.08) and 0.7 (0.44-1.12) respectively].
    2 context sentences
    Summary · context
    In a multicentre, randomized, clinical trial, IVF/ICSI patients were allocated to a standard regimen, in which they received daily 0.25 mg GnRH antagonist ganirelix (Orgalutran) from the 6th day of stimulation onward (fixed regimen n = 102)
    Summary · context
    or to an individualized regimen, in which IVF/ICSI patients received daily 0.25 mg GnRH antagonist starting on the day that the dominant follicle had reached a diameter of > or = 15 mm (flexible regimen n = 103).

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, 16:35 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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