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Effect of Adding Human Chorionic Gonadotropin to The Endometrial Preparation Protocol in Frozen Embryo Transfer Cycles
BACKGROUND: Human chorionic gonadotropin (HCG), one of the initial embryonic signals, is probably a major regulator of the embryo-endometrial relationship. This study aims to assess the advantage of HCG supplementation during the secretory phase of hormonally prepared cycles for the transfer of cryo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850306/ https://www.ncbi.nlm.nih.gov/pubmed/24520435 |
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author | Eftekhar, Maryam Rahmani, Elham Eftekhar, Tahereh |
author_facet | Eftekhar, Maryam Rahmani, Elham Eftekhar, Tahereh |
author_sort | Eftekhar, Maryam |
collection | PubMed |
description | BACKGROUND: Human chorionic gonadotropin (HCG), one of the initial embryonic signals, is probably a major regulator of the embryo-endometrial relationship. This study aims to assess the advantage of HCG supplementation during the secretory phase of hormonally prepared cycles for the transfer of cryopreserved-thawed embryos. MATERIALS AND METHODS: This study was a randomized clinical trial. Infertile women who were candidates for frozen-thawed embryo transfers entered the study and were divided into two groups, HCG and control. The endometrial preparation method was similar in both groups: all women received estradiol valerate (6 mg) po per day from the second day of the menstrual cycle and progesterone in oil (100 mg) intramuscular (I.M.) when the endometrial thickness reached 8 mm. Estradiol and progesterone were continued until the tenth week of gestation. In the HCG group, patients received an HCG 5000 IU injection on the first day of progesterone administration and the day of embryo transfer. RESULTS: In this study, 130 couples participated: 65 in the HCG group and 65 in the control group. There was no statistically significant difference between groups regarding basic characteristics. Implantation rate, chemical pregnancy, clinical pregnancy, ongoing pregnancy, and abortion rates were similar in both groups. CONCLUSION: Although HCG has some advantages in assisted reproductive technology (ART) cycles, our study did not show any benefit of HCG supplementation during the secretory phase of frozen cycles (Registration Number: IRCT201107266420N4). |
format | Online Article Text |
id | pubmed-3850306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-38503062014-02-11 Effect of Adding Human Chorionic Gonadotropin to The Endometrial Preparation Protocol in Frozen Embryo Transfer Cycles Eftekhar, Maryam Rahmani, Elham Eftekhar, Tahereh Int J Fertil Steril Research Article BACKGROUND: Human chorionic gonadotropin (HCG), one of the initial embryonic signals, is probably a major regulator of the embryo-endometrial relationship. This study aims to assess the advantage of HCG supplementation during the secretory phase of hormonally prepared cycles for the transfer of cryopreserved-thawed embryos. MATERIALS AND METHODS: This study was a randomized clinical trial. Infertile women who were candidates for frozen-thawed embryo transfers entered the study and were divided into two groups, HCG and control. The endometrial preparation method was similar in both groups: all women received estradiol valerate (6 mg) po per day from the second day of the menstrual cycle and progesterone in oil (100 mg) intramuscular (I.M.) when the endometrial thickness reached 8 mm. Estradiol and progesterone were continued until the tenth week of gestation. In the HCG group, patients received an HCG 5000 IU injection on the first day of progesterone administration and the day of embryo transfer. RESULTS: In this study, 130 couples participated: 65 in the HCG group and 65 in the control group. There was no statistically significant difference between groups regarding basic characteristics. Implantation rate, chemical pregnancy, clinical pregnancy, ongoing pregnancy, and abortion rates were similar in both groups. CONCLUSION: Although HCG has some advantages in assisted reproductive technology (ART) cycles, our study did not show any benefit of HCG supplementation during the secretory phase of frozen cycles (Registration Number: IRCT201107266420N4). Royan Institute 2012 2012-12-17 /pmc/articles/PMC3850306/ /pubmed/24520435 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 | Research Article Eftekhar, Maryam Rahmani, Elham Eftekhar, Tahereh Effect of Adding Human Chorionic Gonadotropin to The Endometrial Preparation Protocol in Frozen Embryo Transfer Cycles |
title | Effect of Adding Human Chorionic Gonadotropin to The Endometrial
Preparation Protocol in Frozen Embryo Transfer Cycles |
title_full | Effect of Adding Human Chorionic Gonadotropin to The Endometrial
Preparation Protocol in Frozen Embryo Transfer Cycles |
title_fullStr | Effect of Adding Human Chorionic Gonadotropin to The Endometrial
Preparation Protocol in Frozen Embryo Transfer Cycles |
title_full_unstemmed | Effect of Adding Human Chorionic Gonadotropin to The Endometrial
Preparation Protocol in Frozen Embryo Transfer Cycles |
title_short | Effect of Adding Human Chorionic Gonadotropin to The Endometrial
Preparation Protocol in Frozen Embryo Transfer Cycles |
title_sort | effect of adding human chorionic gonadotropin to the endometrial
preparation protocol in frozen embryo transfer cycles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850306/ https://www.ncbi.nlm.nih.gov/pubmed/24520435 |
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