The addition of growth hormone adjuvant therapy to the long down regulation protocol in poor responders undergoing in vitro fertilization: Randomized control trial

Eur J Obstet Gynecol Reprod Biol. 2018 Sep:228:161-165. doi: 10.1016/j.ejogrb.2018.06.035. Epub 2018 Jun 22.

Abstract

Objective: to detect the impact of growth hormone (GH) co-treatment to the long down regulation protocol, on the outcomes of IVF/ICSI cycles in poor responders.

Study design: this parallel open label randomized control trial was conducted in a university hospital. It included 240 females satisfying the bologna criteria for poor responders. The enrolled females were randomized into 2 groups: A (long/GH) receiving GH adjuvant therapy to the long protocol and group B (control) receiving the long protocol alone. The main outcome measure was the live birth rate (fresh, frozen and cumulative).

Results: GH supplementation improved the number of collected oocytes (5.4 ± 1.7 vs. 4.3 ± 2.1), MII oocytes (4.1 ± 2.1 vs. 2.1 ± 1.4), fertilized oocytes (4.0 ± 2.2 vs. 2.0 ± 1.2), transferred embryos (2.4 ± 0.9 vs. 1.6 ± 1.1) and cryopreserved (0.5 ± 0.7 vs. 0.2 ± 0.5). There was no significant difference in the live birth rate whether fresh (17.5% vs. 14.1%) or cumulative (18.3% vs. 14.7%).

Conclusions: Further studies are needed to know the true impact of adding GH to the induction protocols in poor responders, as there was no difference in the live birth rates between the study groups, indicating a lack of trend toward benefit from GH supplementation in poor responders.

Clinical trial registration: NCT02338206.

Keywords: Growth hormone; In vitro fertilization; Long down regulation protocol; Poor responders.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Birth Rate
  • Female
  • Fertilization in Vitro
  • Human Growth Hormone / administration & dosage*
  • Humans
  • Ovulation Induction / methods*
  • Ovulation Induction / statistics & numerical data
  • Pregnancy

Substances

  • Human Growth Hormone

Associated data

  • ClinicalTrials.gov/NCT02338206