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Pregnancy Rate Following Luteal Phase Support in Iranian Women with Polycystic Ovarian Syndrome

BACKGROUND: To assess the efficacy of luteal phase support (LPS) using intravaginal progesterone (P) on pregnancy rate in Iranian women with polycystic ovarian syndrome (PCOS) who used a combination for ovulation induction consisting of letrozole or clomi- phene citrate (CC) and human menopausal gon...

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Autores principales: Foroozanfard, Fatemeh, Saberi, Hamidreza, Moraveji, Seyed Alireza, Bazarganipour, Fatemeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221508/
https://www.ncbi.nlm.nih.gov/pubmed/25379150
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author Foroozanfard, Fatemeh
Saberi, Hamidreza
Moraveji, Seyed Alireza
Bazarganipour, Fatemeh
author_facet Foroozanfard, Fatemeh
Saberi, Hamidreza
Moraveji, Seyed Alireza
Bazarganipour, Fatemeh
author_sort Foroozanfard, Fatemeh
collection PubMed
description BACKGROUND: To assess the efficacy of luteal phase support (LPS) using intravaginal progesterone (P) on pregnancy rate in Iranian women with polycystic ovarian syndrome (PCOS) who used a combination for ovulation induction consisting of letrozole or clomi- phene citrate (CC) and human menopausal gonadotropin (HMG). MATERIALS AND METHODS: This was a randomized clinical trial undertaken in a fertility clinic in Kashan, Isfahan Province, Iran. A total of 198 patients completed treatment and follow up. Base on chosen ovulation induction programs, they were divided into two following group: i. CC group (n=98) used a combination consisting of CC (100 mg×5 day) and HMG (150 IU×5 day) and ii. letrozole group (n=100) used a combination consisting of letrozole (5 mg×5 day) and HMG (150 IU×5 day). After human chorionic gonadotropin (hCG) administration (5000 IU), the patients (n=122) who randomly re- ceived intravaginal P (Cyclogest, 400 mg daily) were included in LPS group, while the rest (n=123) were included in non-P cycles group. The outcome was the comparison of chemical pregnancy rate between the groups. RESULTS: Our findings showed that LPS was associated with a 10% higher pregnancy rate than in non-P cycles, although this difference did not reach statistical significant (p=0.08). LPS improved pregnancy rate in both CC (4%) and letrozole (6%) groups. In addition, patients who used letrozole for ovulation induction along with intravaginal P showed higher pregnancy rates than CC group. CONCLUSION: Administration of vaginal P for LPS may improve the pregnancy rate in women with PCOS using letrozole or CC in combination with HMG for ovulation induc- tion (Registration Number: IRCT201206072967N4).
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spelling pubmed-42215082014-11-06 Pregnancy Rate Following Luteal Phase Support in Iranian Women with Polycystic Ovarian Syndrome Foroozanfard, Fatemeh Saberi, Hamidreza Moraveji, Seyed Alireza Bazarganipour, Fatemeh Int J Fertil Steril Original Article BACKGROUND: To assess the efficacy of luteal phase support (LPS) using intravaginal progesterone (P) on pregnancy rate in Iranian women with polycystic ovarian syndrome (PCOS) who used a combination for ovulation induction consisting of letrozole or clomi- phene citrate (CC) and human menopausal gonadotropin (HMG). MATERIALS AND METHODS: This was a randomized clinical trial undertaken in a fertility clinic in Kashan, Isfahan Province, Iran. A total of 198 patients completed treatment and follow up. Base on chosen ovulation induction programs, they were divided into two following group: i. CC group (n=98) used a combination consisting of CC (100 mg×5 day) and HMG (150 IU×5 day) and ii. letrozole group (n=100) used a combination consisting of letrozole (5 mg×5 day) and HMG (150 IU×5 day). After human chorionic gonadotropin (hCG) administration (5000 IU), the patients (n=122) who randomly re- ceived intravaginal P (Cyclogest, 400 mg daily) were included in LPS group, while the rest (n=123) were included in non-P cycles group. The outcome was the comparison of chemical pregnancy rate between the groups. RESULTS: Our findings showed that LPS was associated with a 10% higher pregnancy rate than in non-P cycles, although this difference did not reach statistical significant (p=0.08). LPS improved pregnancy rate in both CC (4%) and letrozole (6%) groups. In addition, patients who used letrozole for ovulation induction along with intravaginal P showed higher pregnancy rates than CC group. CONCLUSION: Administration of vaginal P for LPS may improve the pregnancy rate in women with PCOS using letrozole or CC in combination with HMG for ovulation induc- tion (Registration Number: IRCT201206072967N4). Royan Institute 2014 2014-11-01 /pmc/articles/PMC4221508/ /pubmed/25379150 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Foroozanfard, Fatemeh
Saberi, Hamidreza
Moraveji, Seyed Alireza
Bazarganipour, Fatemeh
Pregnancy Rate Following Luteal Phase Support in Iranian Women with Polycystic Ovarian Syndrome
title Pregnancy Rate Following Luteal Phase Support in Iranian Women with Polycystic Ovarian Syndrome
title_full Pregnancy Rate Following Luteal Phase Support in Iranian Women with Polycystic Ovarian Syndrome
title_fullStr Pregnancy Rate Following Luteal Phase Support in Iranian Women with Polycystic Ovarian Syndrome
title_full_unstemmed Pregnancy Rate Following Luteal Phase Support in Iranian Women with Polycystic Ovarian Syndrome
title_short Pregnancy Rate Following Luteal Phase Support in Iranian Women with Polycystic Ovarian Syndrome
title_sort pregnancy rate following luteal phase support in iranian women with polycystic ovarian syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221508/
https://www.ncbi.nlm.nih.gov/pubmed/25379150
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