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Ascorbic Acid Supplement During Luteal Phase in IVF

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Abstract

Purpose: To evaluate the impact of ascorbic acid of different doses as additional support during luteal phase in infertility treatment by means of a prospective, randomized, placebo-controlled, group comparative, double-blind study. Methods: Voluntary daily oral intake of either ascorbic acid (1, 5, or 10 g/day) or Placebo for 14 days after follicle aspiration for IVF-ET procedure. Data was obtained on 620 cases of women, age <40 years, undergoing first IVF-embryo transfer cycles in two private out-patient infertility clinics. All women were stimulated by the same protocol. The mean age was 31.73 (±4.4 SD) years. Results: No differences in clinical pregnancy rate and implantation rate were noted in statistical logistic regression analysis between the four intake groups. Conclusions: There was no clinical evidence of any beneficial effect, as defined by main outcome measures, of ascorbic acid on IVF-ET. Our data suggest there is no obvious value of high dosed intake of vitamin C during luteal phase in infertility treatment.

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Correspondence to Wilfried Feichtinger.

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Griesinger, G., Franke, K., Kinast, C. et al. Ascorbic Acid Supplement During Luteal Phase in IVF. J Assist Reprod Genet 19, 164–168 (2002). https://doi.org/10.1023/A:1014837811353

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  • DOI: https://doi.org/10.1023/A:1014837811353

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