Efficacy of growth hormone supplementation with ultrashort GnRH antagonist in IVF/ICSI for poor responders; randomized controlled trial
Objectives: To compare the ICSI-ET outcomes in poor responders who underwent ovarian stimulation by the ultrashort GnRH antagonist protocol with or without adjuvant GH injection. Material and methods: This randomized controlled study was conducted at Al-Azhar University from December-2018 to June-20...
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doaj-bc719c4e671e404a95960a69fb45b07d2021-01-24T04:26:33ZengElsevierTaiwanese Journal of Obstetrics & Gynecology1028-45592021-01-016015155Efficacy of growth hormone supplementation with ultrashort GnRH antagonist in IVF/ICSI for poor responders; randomized controlled trialEhab H. Mohammad0Ahmed G. Abou El Serour1Eman A.H. Mohamed2Amr H. Abbasy3Mahmoud Zaatar4Kamal A. Rageh5Mohamed M. Shafeek6Emad R. Issak7Department of Gynecology and Obstetrics, Faculty of Medicine, Al-Azhar University, EgyptDepartment of Gynecology and Obstetrics, Faculty of Medicine, Al-Azhar University, EgyptDepartment of Embryology, International Islamic Center for Population Studies & Research, Al Azhar University, EgyptDepartment of Obstetrics & Gynecology, National Research Center, EgyptDepartment of Obstetrics & Gynecology, National Research Center, EgyptDepartment of Gynecology and Obstetrics, Faculty of Medicine, Al-Azhar University, EgyptDepartment of Obstetrics & Gynecology, National Research Center, EgyptDepartment of Internal Medicine, Nova Clinics, Cairo, Egypt; Corresponding author. 47 Becho, Maadi, Cairo, Egypt.Objectives: To compare the ICSI-ET outcomes in poor responders who underwent ovarian stimulation by the ultrashort GnRH antagonist protocol with or without adjuvant GH injection. Material and methods: This randomized controlled study was conducted at Al-Azhar University from December-2018 to June-2019 upon 156 participants. All patients received the same preparations. After randomization, in the study group, women have received GH 4 IU/day subcutaneous injection from the second day of the cycle stopped one day before ovum pickup. While in the control group, women have received subcutaneous saline in the same dosing as in the study group. After intervention, all procedures were the same in both groups. The main outcome measure was the clinical pregnancy rate. Statistical analysis was based on the intention-to-treat population. Results: Both groups were comparable with regard their baseline characteristics (p-values > 0.05). Ovulation characteristics were comparable (p-values > 0.05). The level of E2 is significantly (p-value = 0.003) higher in the GH group. The oocyte retrieved number was significantly (p-value < 0.001) higher in the GH group 4.94 ± 1.77 than in the control group 3.74 ± 1.82. The mean number of MII oocytes was significantly (p-value < 0.001) higher in the GH group 3.3 ± 1.36 than in the control group 2.29 ± 1.24. Fertilization characteristics, implantation rate, pregnancy rate were comparable (p-values > 0.05). Conclusion: Despite the fact that this study showed no significant increase in the clinical and chemical pregnancy rates by the addition of GH to the ultrashort antagonist protocol in poor responders, the number of retrieved oocytes was significantly higher in the GH group. Clinical trial registration: ClinicalTrials.gov Identifier: NCT03759301.http://www.sciencedirect.com/science/article/pii/S1028455920302527Embryo transferGrowth hormoneOvarian inductionOvarian insufficiencyPregnancy rate |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ehab H. Mohammad Ahmed G. Abou El Serour Eman A.H. Mohamed Amr H. Abbasy Mahmoud Zaatar Kamal A. Rageh Mohamed M. Shafeek Emad R. Issak |
spellingShingle |
Ehab H. Mohammad Ahmed G. Abou El Serour Eman A.H. Mohamed Amr H. Abbasy Mahmoud Zaatar Kamal A. Rageh Mohamed M. Shafeek Emad R. Issak Efficacy of growth hormone supplementation with ultrashort GnRH antagonist in IVF/ICSI for poor responders; randomized controlled trial Taiwanese Journal of Obstetrics & Gynecology Embryo transfer Growth hormone Ovarian induction Ovarian insufficiency Pregnancy rate |
author_facet |
Ehab H. Mohammad Ahmed G. Abou El Serour Eman A.H. Mohamed Amr H. Abbasy Mahmoud Zaatar Kamal A. Rageh Mohamed M. Shafeek Emad R. Issak |
author_sort |
Ehab H. Mohammad |
title |
Efficacy of growth hormone supplementation with ultrashort GnRH antagonist in IVF/ICSI for poor responders; randomized controlled trial |
title_short |
Efficacy of growth hormone supplementation with ultrashort GnRH antagonist in IVF/ICSI for poor responders; randomized controlled trial |
title_full |
Efficacy of growth hormone supplementation with ultrashort GnRH antagonist in IVF/ICSI for poor responders; randomized controlled trial |
title_fullStr |
Efficacy of growth hormone supplementation with ultrashort GnRH antagonist in IVF/ICSI for poor responders; randomized controlled trial |
title_full_unstemmed |
Efficacy of growth hormone supplementation with ultrashort GnRH antagonist in IVF/ICSI for poor responders; randomized controlled trial |
title_sort |
efficacy of growth hormone supplementation with ultrashort gnrh antagonist in ivf/icsi for poor responders; randomized controlled trial |
publisher |
Elsevier |
series |
Taiwanese Journal of Obstetrics & Gynecology |
issn |
1028-4559 |
publishDate |
2021-01-01 |
description |
Objectives: To compare the ICSI-ET outcomes in poor responders who underwent ovarian stimulation by the ultrashort GnRH antagonist protocol with or without adjuvant GH injection. Material and methods: This randomized controlled study was conducted at Al-Azhar University from December-2018 to June-2019 upon 156 participants. All patients received the same preparations. After randomization, in the study group, women have received GH 4 IU/day subcutaneous injection from the second day of the cycle stopped one day before ovum pickup. While in the control group, women have received subcutaneous saline in the same dosing as in the study group. After intervention, all procedures were the same in both groups. The main outcome measure was the clinical pregnancy rate. Statistical analysis was based on the intention-to-treat population. Results: Both groups were comparable with regard their baseline characteristics (p-values > 0.05). Ovulation characteristics were comparable (p-values > 0.05). The level of E2 is significantly (p-value = 0.003) higher in the GH group. The oocyte retrieved number was significantly (p-value < 0.001) higher in the GH group 4.94 ± 1.77 than in the control group 3.74 ± 1.82. The mean number of MII oocytes was significantly (p-value < 0.001) higher in the GH group 3.3 ± 1.36 than in the control group 2.29 ± 1.24. Fertilization characteristics, implantation rate, pregnancy rate were comparable (p-values > 0.05). Conclusion: Despite the fact that this study showed no significant increase in the clinical and chemical pregnancy rates by the addition of GH to the ultrashort antagonist protocol in poor responders, the number of retrieved oocytes was significantly higher in the GH group. Clinical trial registration: ClinicalTrials.gov Identifier: NCT03759301. |
topic |
Embryo transfer Growth hormone Ovarian induction Ovarian insufficiency Pregnancy rate |
url |
http://www.sciencedirect.com/science/article/pii/S1028455920302527 |
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