Table 4.
Study | Patients | Protocol | Findings |
---|---|---|---|
Cavalli et al. 2008 [63] | 3 women with at least one previous pregnancy affected by folate-resistant NTD | Open-label treatment with 500 mg per day from at least two months before and until 60 days after conception | NTD incidence: 0% |
Cavalli et al. 2011 [64] | 9 women with at least one previous pregnancy affected by folate-resistant NTD | Open-label treatment with 1000 mg per day from at least two months before and until 60 days after conception | NTD incidence: 0% |
Greene et al. 2016 [65] | 47 randomized and 22 non-randomized women with at least one previous pregnancy affected by NTD | Randomized, double-blind, placebo-controlled treatment with 500 mg twice per day; women who declined randomization decided to take myo-inositol plus folic acid (19 patients), or folic acid only (3 patients) | NTD incidence in randomized patients: 0% in the treatment group versus 5.3% in the control group NTD cases in the non-randomized patients: 0 in the myo-inositol plus folic acid group versus 2 in the folic acid alone group Overall NTD incidence: 0% in the treatment group versus 13.63% in the control group |