Prevention of recurrent spontaneous abortion by intravenous immunoglobulin: a double-blind placebo-controlled study

Hum Reprod. 1999 Mar;14(3):838-41. doi: 10.1093/humrep/14.3.838.

Abstract

The aim of this study was to evaluate the therapeutic efficacy of intravenous immunoglobulin (IVIG) in the prevention of recurrent spontaneous abortion (RSA). In a double-blind, randomized, placebo-controlled study, 41 women with a history of unexplained recurrent spontaneous abortion were treated with IVIG or saline infusions during pregnancy. The birth of a child was considered a successful outcome. The overall success rate was 77% in the IVIG group compared with 79% in the placebo group. For women with primary RSA the success rates were 82 (IVIG) and 89% (placebo), and for women with secondary RSA the rates were 73 (IVIG) and 70% (placebo). We found no statistically significant difference in treatment results between IVIG and placebo.

Publication types

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

MeSH terms

  • Abortion, Habitual / prevention & control*
  • Birth Weight
  • Double-Blind Method
  • Female
  • Gestational Age
  • Humans
  • Immunoglobulins, Intravenous / adverse effects
  • Immunoglobulins, Intravenous / therapeutic use*
  • Infant, Newborn
  • Placebos
  • Pregnancy
  • Treatment Outcome

Substances

  • Immunoglobulins, Intravenous
  • Placebos