IMR Press / CEOG / Volume 26 / Issue 2 / pii/1999025

Clinical and Experimental Obstetrics & Gynecology (CEOG) is published by IMR Press from Volume 47 Issue 1 (2020). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with S.O.G.

Original Research

Ovarian stimulation using a new highly purified urinary FSH: a prospective randomized clinical study

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1 Gynecological and Obstetric Institute, University of Perugia (Italy)
2 Physiopathology of Human Reproduction Department, “Papardo” Hospital, Messina (Italy)
3 Associationfor Infertility Studies, Rome (Italy)
Clin. Exp. Obstet. Gynecol. 1999, 26(2), 93–94;
Published: 10 June 1999
Abstract

The aim of this study was to determine the effectiveness of a new highly purified urinary FSH. A total of 60 in vitro-fertilization (IVF) patients, undergoing embryo transfer (ET) for the first time, were randomly allocated into two groups: Group A (n = 30). Subcutaneous administration of urinary follicle-stimulating hormone (FSH, Fostimon 75, A.M.S.A., Italy). Group B (n = 30). Subcutaneous administration of urinary follicle-stimulating hormone (FSH, Metrodin 75 HP, Serono, Italy). Statistical analysis was performed using the chi-square test, p < 0.05 was assumed as significant. This prospective randomized clinical study in an IVF-ET program showed that both drugs were equally safe and effective. Except for the number of the high quality embryos (3.16 vs 2.9; p = 0.03) the two groups did not differ in stimulation parameters or clinical pregnancy rates per attempt and per transfer. On the other hand, a mean number of 3.56 vs 2.18 embryos were cryopreserved in group A and in group B, respecti­vely, as a result of the high number of mature oocytes and high quality embryos. When frozen embryo cycles were included, the difference in pregnancy rate became significant.

Keywords
FSH
Effectiveness
Fostimon
Metrodin HP
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