Improvement in early human embryo development using new formulation sequential stage-specific culture media

Fertil Steril. 2002 Dec;78(6):1254-60. doi: 10.1016/s0015-0282(02)04343-1.

Abstract

Objective: To determine whether altering selected components of sequential culture media can improve early development variables of human embryos.

Design: Prospective, randomized, sibling oocyte split trial.

Setting: Private ART center.

Patient(s): Two hundred eight undergoing treatment with in vitro fertilization or microinjection.

Intervention(s): Oocytes from each patient were randomly allocated to fertilization and cleavage media of a control and a trial culture medium formulation.

Main outcome measure(s): Rates of fertilization, cleavage, and uncontrolled division; average embryo morphology score; blastomeres per embryo; embryo score parameter (number of blastomeres x embryo morphology grade); and embryo utilization. The trial media resulted in a higher fertilization rate, higher cleavage rate, lower rate of uncontrolled division, higher number of blastomeres per embryo, higher average embryo morphology score, a higher embryo score parameter, and higher embryo utilization rate compared to the control media. All differences were statistically significant.

Conclusion(s): Improved sequential stage-specific culture media can reduce the occurrence of severe human embryo fragmentation and improve developmental variables in early IVF- and ICSI-generated embryos.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Blastomeres / drug effects
  • Body Fluids / physiology
  • Cell Division / drug effects
  • Cleavage Stage, Ovum / drug effects
  • Culture Media / chemistry*
  • Culture Media / pharmacology*
  • Embryo, Mammalian / anatomy & histology
  • Embryonic and Fetal Development / drug effects*
  • Fallopian Tubes / metabolism
  • Female
  • Fertilization / drug effects
  • Fertilization in Vitro*
  • Humans
  • Pregnancy
  • Prospective Studies
  • Sperm Injections, Intracytoplasmic*

Substances

  • Culture Media