Clinical outcome of one-third-dose depot triptorelin is the same as half-dose depot triptorelin in the long protocol of controlled ovarian stimulation
Objective: Appropriate dosage of the long-acting depot gonadotrophin releasing hormone (GnRH) agonist has not been determined in long protocol for IVF, and one-third-dose depot triptorelin was compared with half-dose in a luteal long protocol of in-vitro fertilization/ intra cytoplasmic sperm inject...
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Wolters Kluwer Medknow Publications,
2012-01-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_7622b9e22d1e4b14ab90661d6d7aa6e1 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Yu Li |e author |
700 | 1 | 0 | |a Dongzi Yang |e author |
700 | 1 | 0 | |a Qingxue Zhang |e author |
245 | 0 | 0 | |a Clinical outcome of one-third-dose depot triptorelin is the same as half-dose depot triptorelin in the long protocol of controlled ovarian stimulation |
260 | |b Wolters Kluwer Medknow Publications, |c 2012-01-01T00:00:00Z. | ||
500 | |a 0974-1208 | ||
500 | |a 1998-4766 | ||
500 | |a 10.4103/0974-1208.97785 | ||
520 | |a Objective: Appropriate dosage of the long-acting depot gonadotrophin releasing hormone (GnRH) agonist has not been determined in long protocol for IVF, and one-third-dose depot triptorelin was compared with half-dose in a luteal long protocol of in-vitro fertilization/ intra cytoplasmic sperm injection (IVF/ICSI) treatment in this study. Materials and Methods: This is a prospective, randomized, open clinical trial. 100 patients were randomized into two groups. Group I received one-third-dose (1.25 mg) depot triptorelin. Group II received half-dose (1.87 mg). The clinical and experimental parameters were compared between the two groups. Results: There was no premature luteinizing hormone (LH) surge in both groups. On Day 3-5 of menstrual cycle after down-regulation, fewer patients showed low-level LH (<1.0 IU/L) and estradiol (<30 pg/mL) in group I (P <0.05). There were fewer oocytes retrieved (P =0.086), fewer total embryos and available embryos for cryopreservation in Group I (P <0.05), while good-quality embryo rate was higher in group I (P <0.05). The length and dose of ovarian stimulation was lower in Group I, but not significantly. The clinical pregnancy (52% versus 40%), implantation (48% versus 37.5%), delivery (46% versus 32%), or live birth (42% versus 32%) rates and the abortion (8% versus 20%) rates showed no significant differences. Conclusion: Depot triptorelin 1.25 mg can be successfully used with reduced pituitary suppression and lower cost in a long protocol for in-vitro fertilization. | ||
546 | |a EN | ||
690 | |a GnRH agonist | ||
690 | |a in-vitro fertilization | ||
690 | |a ovarian stimulation | ||
690 | |a triptorelin | ||
690 | |a Gynecology and obstetrics | ||
690 | |a RG1-991 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Journal of Human Reproductive Sciences, Vol 5, Iss 1, Pp 14-19 (2012) | |
787 | 0 | |n http://www.jhrsonline.org/article.asp?issn=0974-1208;year=2012;volume=5;issue=1;spage=14;epage=19;aulast=Li | |
787 | 0 | |n https://doaj.org/toc/0974-1208 | |
787 | 0 | |n https://doaj.org/toc/1998-4766 | |
856 | 4 | 1 | |u https://doaj.org/article/7622b9e22d1e4b14ab90661d6d7aa6e1 |z Connect to this object online. |