Synchronization of ovarian stimulation with follicle wave emergence in patients undergoing in vitro fertilization with a prior suboptimal response: a randomized, controlled trial

Fertil Steril. 2012 Oct;98(4):881-7.e1-2. doi: 10.1016/j.fertnstert.2012.06.051. Epub 2012 Jul 20.

Abstract

Objective: To test the hypothesis that synchronizing initiation of ovarian stimulation with follicle wave emergence would optimize IVF/intracytoplasmic sperm injection (ICSI) outcomes in patients with a prior suboptimal response.

Design: Prospective, randomized, controlled trial.

Setting: Academic and private reproductive endocrinology and infertility centers.

Patient(s): Eighty women ≤ 43 years of age with a history of a suboptimal response.

Intervention(s): Initiation of recombinant FSH/GnRH antagonist/recombinant LH/hCG on day 1 (n = 39) or day 4 (n = 41).

Main outcome measure(s): Numbers of clinical and biochemical pregnancies, follicles ≥ 10 and ≥ 15 mm, oocytes collected, fertilized oocytes, cleavage stage embryos, and blastocysts; serum E(2) concentrations. Outcomes were compared between treatment groups.

Result(s): The numbers of follicles that developed to ≥ 10 and ≥ 15 mm and serum E(2) were greater when recombinant FSH was initiated on day 1 (5.4, 4.3, 5,827.2 pmol/L) versus day 4 (3.6, 2.5, 4,230.1 pmol/L). The numbers of collected, metaphase II, and fertilized oocytes; cleavage stage embryos; and blastocysts were not different between groups. When we evaluated only those cycles that proceeded to oocyte pick-up, a lower implantation rate (16.1%, 56.0%), biochemical pregnancy rate (PR) (16.1%, 48.0%), and clinical PR (12.9% vs. 36.0%) were detected in the day 1 group versus day 4 group.

Conclusion(s): Synchronizing initiation of ovarian stimulation with follicle wave emergence in patients with a prior suboptimal response resulted in an increase in the number of dominant follicles and serum E(2) concentrations; however, improvements in oocyte, embryo, or pregnancy outcomes did not occur.

Clinical trial registration number: NCT00439829.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Fertilization in Vitro / methods*
  • Follicle Stimulating Hormone, Human / administration & dosage
  • Gonadotropin-Releasing Hormone / antagonists & inhibitors
  • Humans
  • Luteinizing Hormone / administration & dosage
  • Oocyte Retrieval / methods
  • Ovarian Follicle / physiology*
  • Ovulation Induction / methods*
  • Pregnancy
  • Pregnancy Rate
  • Prospective Studies
  • Recombinant Proteins / administration & dosage
  • Sperm Injections, Intracytoplasmic / methods*
  • Time Factors

Substances

  • Follicle Stimulating Hormone, Human
  • Recombinant Proteins
  • Gonadotropin-Releasing Hormone
  • Luteinizing Hormone

Associated data

  • ClinicalTrials.gov/NCT00439829