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...

Full description

Saved in:
Bibliographic Details
Main Authors: Yu Li (Author), Dongzi Yang (Author), Qingxue Zhang (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2012-01-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
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.