The inSIGHT study: costs and effects of routine hysteroscopy prior to a first IVF treatment cycle. A randomised controlled trial.
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Smit Janine G, Kasius Jenneke C, Eijkemans Marinus J C, Koks Carolien A M, Van Golde Ron, Oosterhuis Jurjen G E, Nap Annemiek W, Scheffer Gabrielle J, Manger Petra A P, Hoek Annemiek, Kaplan Mesrure, Schoot Dick B C, van Heusden Arne M, Kuchenbecker Walter K H, Perquin Denise A M, Fleischer Kathrin, Kaaijk Eugenie M, Sluijmer Alexander, Friederich Jaap, Laven Joop S E, van Hooff Marcel, Louwe Leonie A, Kwee Janet, Boomgaard Jantien J, de Koning Corry H, Janssen Ineke C A H, Mol Femke, Mol Ben W J, Torrance Helen L, Broekmans Frank J M
Аннотация
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.