In this study, female patients diagnosed with polycystic ovary syndrome (PCOS) will be enrolled. In particular, those with elevated testosterone or with clinical signs of hyperandrogenism, along with menstrual cycle alterations and/or polycystic ovary morphology at ultrasound, will be included in the study. Current treatments for PCOS include insulin sensitizers (such as metformin) and hormonal contraceptives. However, they are not devoid of side effects or may not be well tolerated, often leading to therapy discontinuation. Inositol represents a valid alternative to standard treatments, as it serves both as insulin sensitizer and as second messenger of FSH in the ovaries, thus regulating glucose metabolism and supporting ovarian function. The presence of two inositol isomers, namely myo-inositol and D-chiro-inositol, in defined ratios in human tissues suggests that supplementation with both would be ideal. Despite numerous evidence available, the ratio that gives the best clinical results is still debated. In the present clinical trial, patients will be given a dietary supplement containing myo-inositol and D-chiro-inositol in two ratios (either 40:1 or 3.6:1, respectively) for three months. Restoration of regular menstrual cycle and of hormonal status will be the primary goal of the intervention.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Myo-inositol and D-chiro-inositol (40:1 ratio), 2 grams (twice a day) for three months
Myo-inositol and D-chiro-inositol (3.6:1 ratio), 1.4 grams (once daily) for three months
Alma Res Fertility Center
Rome, ITA, Italy
Restoration of regular menstrual cycle
Number (%) of patients with regular menstrual cycle at the end of the study
Time frame: From enrollment (T0) to the completion of the study at 3 months (T3M)
Hormonal status
Changes of serum hormonal levels (Progesterone; FSH; LH; Estradiol; Testosterone; Insulin)
Time frame: From enrollment (T0) to the completion of the study at 3 months (T3M)
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