The inSIGHT study: costs and effects of routine hysteroscopy prior to a first IVF treatment cycle. A randomised controlled trial

BMC Womens Health. 2012 Aug 8:12:22. doi: 10.1186/1472-6874-12-22.

Abstract

Background: In in vitro fertilization (IVF) and intracytoplasmatic sperm injection (ICSI) treatment a large drop is present between embryo transfer and occurrence of pregnancy. The implantation rate per embryo transferred is only 30%. Studies have shown that minor intrauterine abnormalities can be found in 11-45% of infertile women with a normal transvaginal sonography or hysterosalpingography. Two randomised controlled trials have indicated that detection and treatment of these abnormalities by office hysteroscopy after two failed IVF cycles leads to a 9-13% increase in pregnancy rate. Therefore, screening of all infertile women for intracavitary pathology prior to the start of IVF/ICSI is increasingly advocated. In absence of a scientific basis for such a policy, this study will assess the effects and costs of screening for and treatment of unsuspected intrauterine abnormalities by routine office hysteroscopy, with or without saline infusion sonography (SIS), prior to a first IVF/ICSI cycle.

Methods/design: Multicenter randomised controlled trial in asymptomatic subfertile women, indicated for a first IVF/ICSI treatment cycle, with normal findings at transvaginal sonography. Women with recurrent miscarriages, prior hysteroscopy treatment and intermenstrual blood loss will not be included. Participants will be randomised for a routine fertility work-up with additional (SIS and) hysteroscopy with on-the-spot-treatment of predefined intrauterine abnormalities versus the regular fertility work-up without additional diagnostic tests. The primary study outcome is the cumulative ongoing pregnancy rate resulting in live birth achieved within 18 months of IVF/ICSI treatment after randomisation. Secondary study outcome parameters are the cumulative implantation rate; cumulative miscarriage rate; patient preference and patient tolerance of a SIS and hysteroscopy procedure. All data will be analysed according to the intention-to-treat principle, using univariate and multivariate logistic regression and cox regression. Cost-effectiveness analysis will be performed to evaluate the costs of the additional tests as routine procedure. In total 700 patients will be included in this study.

Discussion: The results of this study will help to clarify the significance of hysteroscopy prior to IVF treatment.

Trial registration: NCT01242852.

Publication types

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

MeSH terms

  • Clinical Protocols
  • Cost-Benefit Analysis
  • Female
  • Fertilization in Vitro*
  • Humans
  • Hysteroscopy* / economics
  • Infertility, Female / diagnostic imaging
  • Infertility, Female / economics
  • Infertility, Female / etiology
  • Infertility, Female / therapy*
  • Intention to Treat Analysis
  • Logistic Models
  • Multivariate Analysis
  • Netherlands
  • Patient Preference
  • Pregnancy
  • Pregnancy Rate
  • Proportional Hazards Models
  • Single-Blind Method
  • Sperm Injections, Intracytoplasmic
  • Treatment Outcome
  • Ultrasonography
  • Uterine Diseases / complications
  • Uterine Diseases / diagnosis*
  • Uterine Diseases / diagnostic imaging
  • Uterine Diseases / economics
  • Uterus / abnormalities*
  • Uterus / diagnostic imaging

Associated data

  • ClinicalTrials.gov/NCT01242852