Introduce an optimal method of ovarian stimulation in the polycystic ovarian syndrome affected: a randomized controlled trial.


Journal

BMC women's health
ISSN: 1472-6874
Titre abrégé: BMC Womens Health
Pays: England
ID NLM: 101088690

Informations de publication

Date de publication:
20 06 2023
Historique:
received: 14 09 2022
accepted: 10 06 2023
medline: 22 6 2023
pubmed: 21 6 2023
entrez: 20 6 2023
Statut: epublish

Résumé

Currently, optimal method of ovarian stimulation (OS) to in-vitro fertilization (IVF) in the patients with polycystic ovarian syndrome (PCOS) is unknown. The present research aims to study the efficiency of minimal-OS method in treatment of infertile patients with PCOS and also the effect of gonadotropin type (recombinant FSH (r-FSH) vs. urinary Human menopausal gonadotropin (u-HMG)) on treatment cycles with GnRH-antagonist. In this randomized controlled trial, a total of 120 eligible patients were randomly allocated into four groups of OS to IVF: minimal-OS with r-FSH, minimal-OS with u-HMG, mild-OS with r-FSH and mild-OS with u-HMG. IVF outcomes of groups were analyzed statically. The statistical analysis showed that there were significant differences among groups regarding stimulation duration (p < 0.0001), number of retrieved oocytes (p < 0.0001), number of obtained embryos (p < 0.0001). There were no statistically significant differences in fertilization rate (p = 0.289) and implantation rate (p = 0.757) among our participants. There were also significant differences among these four groups in terms of clinical pregnancy rate (/ET and /cycles) (p < 0.0001, p = 0.021, respectively) and live birth rate/cycles (p < 0.0001). Also cases of freeze all embryos due to prevention of ovarian hyper stimulation syndrome (OHSS) (p = 0.004). On the basis of present results the minimal-OS with u-HMG may be one of optimal methods of control OS in the patients with PCOS in respect to serum levels of estradiol on the day of triggering final oocyte maturation, total dose of prescribed gonadotropin, the optimal number of oocytes and embryos obtained, rate of clinical pregnancy and the incidence of OHSS risk. NCT, NCT03876145. Registered 15/03/2019. Retrospectively registered, http://www. gov/ NCT03876145.

Sections du résumé

BACKGROUND
Currently, optimal method of ovarian stimulation (OS) to in-vitro fertilization (IVF) in the patients with polycystic ovarian syndrome (PCOS) is unknown. The present research aims to study the efficiency of minimal-OS method in treatment of infertile patients with PCOS and also the effect of gonadotropin type (recombinant FSH (r-FSH) vs. urinary Human menopausal gonadotropin (u-HMG)) on treatment cycles with GnRH-antagonist.
METHODS
In this randomized controlled trial, a total of 120 eligible patients were randomly allocated into four groups of OS to IVF: minimal-OS with r-FSH, minimal-OS with u-HMG, mild-OS with r-FSH and mild-OS with u-HMG. IVF outcomes of groups were analyzed statically.
RESULTS
The statistical analysis showed that there were significant differences among groups regarding stimulation duration (p < 0.0001), number of retrieved oocytes (p < 0.0001), number of obtained embryos (p < 0.0001). There were no statistically significant differences in fertilization rate (p = 0.289) and implantation rate (p = 0.757) among our participants. There were also significant differences among these four groups in terms of clinical pregnancy rate (/ET and /cycles) (p < 0.0001, p = 0.021, respectively) and live birth rate/cycles (p < 0.0001). Also cases of freeze all embryos due to prevention of ovarian hyper stimulation syndrome (OHSS) (p = 0.004).
CONCLUSIONS
On the basis of present results the minimal-OS with u-HMG may be one of optimal methods of control OS in the patients with PCOS in respect to serum levels of estradiol on the day of triggering final oocyte maturation, total dose of prescribed gonadotropin, the optimal number of oocytes and embryos obtained, rate of clinical pregnancy and the incidence of OHSS risk.
TRIAL REGISTRATION
NCT, NCT03876145. Registered 15/03/2019. Retrospectively registered, http://www.
CLINICALTRIAL
gov/ NCT03876145.

Identifiants

pubmed: 37340371
doi: 10.1186/s12905-023-02473-2
pii: 10.1186/s12905-023-02473-2
pmc: PMC10283261
doi:

Substances chimiques

Gonadotropin-Releasing Hormone 33515-09-2
Gonadotropins 0
Follicle Stimulating Hormone 9002-68-0

Banques de données

ClinicalTrials.gov
['NCT03876145']

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

323

Informations de copyright

© 2023. The Author(s).

Références

Hum Reprod. 2019 Feb 1;34(2):388
pubmed: 30521039
Hum Reprod Open. 2019 Jan 04;2019(1):hoy021
pubmed: 31486807
Hum Reprod. 2007 Apr;22(4):980-8
pubmed: 17204525
Arch Gynecol Obstet. 2010 Apr;281(4):741-6
pubmed: 19834718
J Assist Reprod Genet. 2012 Dec;29(12):1343-51
pubmed: 23086704
Hum Reprod. 2007 Nov;22(11):2801-4
pubmed: 17855409
Fertil Steril. 2012 Mar;97(3):561-71
pubmed: 22244781
Hum Reprod. 2008 Oct;23(10):2346-51
pubmed: 18583332
Am J Obstet Gynecol. 2016 Jan;214(1):96.e1-8
pubmed: 26259908
Fertil Steril. 2016 Aug;106(2):363-370.e3
pubmed: 27172401
Reprod Biol Endocrinol. 2014 Jan 29;12:10
pubmed: 24476504
Methods Mol Biol. 2014;1154:305-28
pubmed: 24782016
Fertil Steril. 2015 Aug;104(2):333-8
pubmed: 26051093
Hum Reprod. 2006 Dec;21(12):3217-27
pubmed: 16873892
Hum Reprod Update. 2009 Jan-Feb;15(1):5-12
pubmed: 19091754
Reprod Biol Endocrinol. 2010 Sep 16;8:112
pubmed: 20846363
Int J Endocrinol. 2015;2015:385049
pubmed: 25866508
Fertil Steril. 2011 Jun 30;95(8):2449-55
pubmed: 21550037
Cochrane Database Syst Rev. 2012 Nov 14;11:CD008528
pubmed: 23152261
Hum Reprod. 2007 Sep;22(9):2404-13
pubmed: 17640944
Hum Reprod. 2008 Feb;23(2):310-5
pubmed: 18056719
Hum Reprod. 2004 Jan;19(1):41-7
pubmed: 14688154
Arch Gynecol Obstet. 2013 Apr;287(4):779-90
pubmed: 23250342
J Endocrinol Invest. 2014 Jan;37(1):65-70
pubmed: 24464452

Auteurs

Azar Yahyaei (A)

Department of Endocrinology and Female Infertility, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.

Samira Vesali (S)

Reproductive Epidemiology Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.

Firouzeh Ghaffari (F)

Department of Endocrinology and Female Infertility, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran. ghafaryf@yahoo.com.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH