1991
DOI: 10.1016/0020-7292(91)90370-k
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The luteal phase in polycystic ovary syndrome during ovulation induction with human menopausal gonadotropin with human menopausal gonadotropin with and without leuprolide acetate

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Cited by 3 publications
(4 citation statements)
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“…The findings in this study are in contrast with earlier studies in normogonadotrophic anovulatory WHO group II women, which have concluded that the serum concentration of progesterone in the mid-luteal phase cannot be used to predict treatment outcome in gonadotrophin-or clomiphene citrate-induced cycles (Laufer et al, 1982;Bachus et al, 1990;Maclin et al, 1990;Ellenbogen et al, 1995). Figure 1 Live birth rates for all women as well as women with large follicles (15 mm) but no medium-sized follicles (12-14 mm) at end of stimulation according to their serum concentrations of progesterone in the mid-luteal phase.…”
Section: Discussioncontrasting
confidence: 99%
See 1 more Smart Citation
“…The findings in this study are in contrast with earlier studies in normogonadotrophic anovulatory WHO group II women, which have concluded that the serum concentration of progesterone in the mid-luteal phase cannot be used to predict treatment outcome in gonadotrophin-or clomiphene citrate-induced cycles (Laufer et al, 1982;Bachus et al, 1990;Maclin et al, 1990;Ellenbogen et al, 1995). Figure 1 Live birth rates for all women as well as women with large follicles (15 mm) but no medium-sized follicles (12-14 mm) at end of stimulation according to their serum concentrations of progesterone in the mid-luteal phase.…”
Section: Discussioncontrasting
confidence: 99%
“…In reality, however, the only means for confirming ovulation is if a pregnancy occurs as no definitive diagnostic test of ovulation is available. Only a few studies have investigated the relationship between mid-luteal serum progesterone concentrations above that used as cut-off for defining ovulation and the chance of pregnancy in anovulatory World Health Organization (WHO) group II women undergoing ovulation-induction treatment, and none of these was able to demonstrate a positive association (Laufer et al, 1982;Bachus et al, 1990;Maclin et al, 1990;Ellenbogen et al, 1995). One of the reasons could be that the earlier studies did not analyse the results in relation to the number of follicles present.…”
Section: Introductionmentioning
confidence: 99%
“…In some cases, authors re‐publish the same trial but with further information, such as a larger number of patients or other outcome variables (Valimaki et al 1989; Ylikorkala et al 1990; Thomas & Cooke 1987b; Cooke & Thomas 1989; Fedele et al 1989b, 1990; Dodson et al 1989; Bachus et al 1990) or an expansion of the original sample (Dodson et al 1987, 1989). Factorial design trials, in which the same group of patients is randomised more than once, were registered as a single trial, but the different interventions are analysed separately.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, combined therapy was associated with an increased risk of OHSS (95-99), but there are insufficient data to draw solid conclusions on miscarriage and multiple pregnancy rates (100)(101)(102). Therefore, the significantly higher hyperstimulation rate, the associated risk of multiple pregnancies, and the additional inconvenience and cost of concomitant GnRH agonist administration, in the absence of documented increases in pregnancy success, do not justify the routine use of GnRH agonists during ovulation induction with gonadotropins in PCOS patients.…”
Section: Combination Of Gnrh Analogues and Gonadotropinsmentioning
confidence: 96%