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Study · Non-randomized trial · n = 61 · 2015

6 results

Three-month treatment with triptorelin, letrozole and ulipristal acetate before hysteroscopic resection of uterine myomas: prospective comparative pilot study.

Bizzarri N, Ghirardi V, Remorgida V, Venturini PL, Ferrero S

European journal of obstetrics, gynecology, and reproductive biology25 Jun 2015Cited by 29 (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 trialOther

    In women with myomas, complications, postoperative pain and satisfaction were similar across triptorelin, letrozole, ulipristal acetate and direct-surgery groups.

    In plain wordsWomen had similar complications, postoperative pain and satisfaction with triptorelin, letrozole, ulipristal acetate or direct surgery.

    Outcome
    No significant changePerioperative complications, pain and satisfaction
    Study

    n = 61

    Comparator
    Direct surgery, letrozole, and ulipristal acetate groups
    Outcome group
    Surgical outcomes · Whole body
    Studied dose
    3.75 mg every 28 days · 3 monthsAs given in this study (human).

    Source sentences

    Summary
    Intra- and postoperative complications, postoperative pain, and patient satisfaction were similar in the four study groups.
    3 context sentences
    Summary · context
    Single center prospective non-randomized comparative pilot study.
    Summary · context
    The study included consecutive premenopausal patients undergoing hysteroscopic resection of myomas graded as type 0, type 1 or type 2 according to the FIGO classification with diameter between 20 and 35 mm.
    Summary · context
    This study enrolled patients who underwent either direct surgery (group S; n=23) or 3-month preoperative treatment with triptorelin (3.75 mg every 28 days; group T; n=20)
  2. 02HumanNon-randomized trialEfficacy outcome

    In women with myomas, preoperative triptorelin reduced hysteroscopy time compared with direct surgery.

    In plain wordsWomen receiving triptorelin had shorter hysteroscopy times than women undergoing direct surgery.

    Outcome
    DecreaseHysteroscopy time
    Study

    n = 43

    Comparator
    Direct surgery
    Outcome group
    Surgical outcomes · Reproductive and sexual health
    Studied dose
    3.75 mg every 28 days · 3 monthsAs given in this study (human).

    Source sentences

    Summary
    The hysteroscopy time was higher in group S than in group T (p<.001) and in group L (p=.001);
    3 context sentences
    Summary · context
    Single center prospective non-randomized comparative pilot study.
    Summary · context
    The study included consecutive premenopausal patients undergoing hysteroscopic resection of myomas graded as type 0, type 1 or type 2 according to the FIGO classification with diameter between 20 and 35 mm.
    Summary · context
    This study enrolled patients who underwent either direct surgery (group S; n=23) or 3-month preoperative treatment with triptorelin (3.75 mg every 28 days; group T; n=20)
  3. 03HumanNon-randomized trialEfficacy outcome

    In women with myomas, preoperative triptorelin reduced fluid absorption compared with direct surgery.

    In plain wordsWomen receiving triptorelin absorbed less fluid during surgery than women undergoing direct surgery.

    Outcome
    DecreaseFluid absorption
    Study

    n = 43

    Comparator
    Direct surgery
    Outcome group
    Surgical outcomes · Reproductive and sexual health
    Studied dose
    3.75 mg every 28 days · 3 monthsAs given in this study (human).

    Source sentences

    Summary
    Fluid absorption was lower in group T than in group S (p=.002) and in group L than in group S (p=.048);
    3 context sentences
    Summary · context
    Single center prospective non-randomized comparative pilot study.
    Summary · context
    The study included consecutive premenopausal patients undergoing hysteroscopic resection of myomas graded as type 0, type 1 or type 2 according to the FIGO classification with diameter between 20 and 35 mm.
    Summary · context
    This study enrolled patients who underwent either direct surgery (group S; n=23) or 3-month preoperative treatment with triptorelin (3.75 mg every 28 days; group T; n=20)
  4. 04HumanNon-randomized trialEfficacy outcome

    In women with myomas, surgeons rated operative difficulty more favorably after triptorelin than with direct surgery.

    In plain wordsSurgeons rated surgery easier after triptorelin than with direct surgery in women with myomas.

    Outcome
    DecreaseOperative difficulty evaluation
    Study

    n = 43

    Comparator
    Direct surgery
    Outcome group
    Surgical outcomes · Reproductive and sexual health
    Studied dose
    3.75 mg every 28 days · 3 monthsAs given in this study (human).

    Source sentences

    Summary
    Surgeon's evaluation of operative difficulty was better in group T than in group S (p<.005).
    3 context sentences
    Summary · context
    Single center prospective non-randomized comparative pilot study.
    Summary · context
    The study included consecutive premenopausal patients undergoing hysteroscopic resection of myomas graded as type 0, type 1 or type 2 according to the FIGO classification with diameter between 20 and 35 mm.
    Summary · context
    This study enrolled patients who underwent either direct surgery (group S; n=23) or 3-month preoperative treatment with triptorelin (3.75 mg every 28 days; group T; n=20)
  5. 05HumanNon-randomized trialEfficacy outcome

    In premenopausal women with myomas, triptorelin produced a greater percentage volume reduction than ulipristal acetate.

    In plain wordsWomen receiving triptorelin had greater myoma shrinkage than those receiving ulipristal acetate.

    Outcome
    IncreaseMyoma volume reduction
    Study

    n = 27

    Comparator
    Ulipristal acetate
    Outcome group
    Tumor growth · Reproductive and sexual health
    Studied dose
    3.75 mg every 28 days · 3 monthsAs given in this study (human).

    Source sentences

    Summary
    however, the percentage decrease in myoma volume was lower in group U than in group T (p=.001) and in group L (p=.010).
    3 context sentences
    Summary · context
    Single center prospective non-randomized comparative pilot study.
    Summary · context
    The study included consecutive premenopausal patients undergoing hysteroscopic resection of myomas graded as type 0, type 1 or type 2 according to the FIGO classification with diameter between 20 and 35 mm.
    Summary · context
    This study enrolled patients who underwent either direct surgery (group S; n=23) or 3-month preoperative treatment with triptorelin (3.75 mg every 28 days; group T; n=20)
  6. 06HumanNon-randomized trialEfficacy outcome

    In premenopausal women with submucosal myomas, triptorelin reduced myoma volume from baseline.

    In plain wordsWomen with submucosal myomas had smaller myomas after triptorelin than at baseline.

    Outcome
    DecreaseMyoma volume
    Study

    n = 20

    Outcome group
    Tumor growth · Reproductive and sexual health
    Studied dose
    3.75 mg every 28 days · 3 monthsAs given in this study (human).

    Source sentences

    Summary
    All medical treatments caused a significant decrease in the volume of myomas (group T, p<.001; group L, p<.001; group U, p=.006)
    3 context sentences
    Summary · context
    Single center prospective non-randomized comparative pilot study.
    Summary · context
    The study included consecutive premenopausal patients undergoing hysteroscopic resection of myomas graded as type 0, type 1 or type 2 according to the FIGO classification with diameter between 20 and 35 mm.
    Summary · context
    This study enrolled patients who underwent either direct surgery (group S; n=23) or 3-month preoperative treatment with triptorelin (3.75 mg every 28 days; group T; n=20)

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

    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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