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Clinical Trials/NCT03598374
NCT03598374
Not yet recruiting
Not Applicable

Effects of Oral Inositol Supplementation on Spontaneous Reproductive Outcomes in Infertile Polycystic Ovarian Syndrome Women.

Università degli Studi dell'Insubria0 sites80 target enrollmentJanuary 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Polycystic Ovarian Syndrome
Sponsor
Università degli Studi dell'Insubria
Enrollment
80
Primary Endpoint
Miscarriage rate
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

Polycystic ovarian syndrome (PCOS) is a heterogeneous, multifaceted and complex disorder characterized by insulin resistance (IR), hyperinsulinemia, and hyperandrogenism leading ovarian disfunction and infertility. Given the central pathogenic role of IR in the endocrine, reproductive, and metabolic disturbances of PCOS, several pharmacological and non-pharmacological approaches have been proposed to counteract the hyper insulinemic IR typical of the syndrome. Two Inositol stereoisomers, Myo-Inositol (MI) and D-chiro-inositol (DCI), captured the attention of researchers for their insulin-sensitizing actions, which configure them as proper candidates for the treatment of PCOS.

Very few studies reported on spontaneous clinical pregnancy rates, none were powered for this outcome, and none reported on the clinically relevant outcome of live birth. Therefore, data about clinical pregnancy rate, live birth rate, and miscarriage rate comparing inositols with placebo are limited.

Conversely, about infertility and assisted reproduction techniques (ART), improvements have been reported in PCOS women who underwent fertility treatment using inositol in different forms, combinations or doses. This data, considering the different tissue-specific ratios (i.e., 100:1 in the ovary) and the different physiological roles of inositol stereoisomers, suggest that DCI supplementation alone might not be the optimal or appropriate approach for improving IVF outcomes in PCOS patients, and drawn attention to the importance of MI and DCI supplementation in a physiological ratio in order to restore normal ovary functionality. Indeed, the combination of MI and DCI, at a more physiological ratio of 40:1, was able to more quickly restore to normal the hormonal and metabolic parameters in PCOS women than MI treatment alone or DCI treatment alone, improving the endocrine profile and IR of women with PCOS.

Nevertheless, regarding infertility the primary outcomes that should be considered are clinical pregnancy rate, miscarriage rate and live birth rate. Although many studies showed improved hormonal and metabolic profile and improved ovulation rate and higher quality and number of oocyte retrieved in ART in PCOS women after inositols administration, data about clinical pregnancy rate, live birth rate, and miscarriage rate are limited with several concerns regarding interpretation of the studies.

Registry
clinicaltrials.gov
Start Date
January 1, 2022
End Date
December 31, 2024
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Università degli Studi dell'Insubria
Responsible Party
Principal Investigator
Principal Investigator

Antonio Simone Laganà

Principal Investigator

Università degli Studi dell'Insubria

Eligibility Criteria

Inclusion Criteria

  • Women with PCOS diagnosed by Rotterdam criteria in couple that desire to conceive.

Exclusion Criteria

  • Male infertility factor that require in vitro fertilization technique.
  • Women with infertility factors that require in vitro fertilization technique.
  • Couple with infertility factors that require in vitro fertilization technique.
  • Diabetes mellitus that require insulin or oral drugs treatment.
  • Any other pre-pregnancy or pregnancy-induced/related disease.
  • Any other pharmacological, non-pharmacological or nutraceutical treatment (beside oral folic acid supplementation) more than 3 months before the enrollment (wash-out period) or during the trial.

Outcomes

Primary Outcomes

Miscarriage rate

Time Frame: Within 6 months from the enrollment

Number of spontaneous abortion per women diagnosed by positive pregnancy test with subsequent spontaneous interruption of the pregnancy.

Live birth rate

Time Frame: Within 18 months from the enrollment

Number of spontaneous pregnancies per women resulted in a delivered viable fetus.

Clinical pregnancy rate

Time Frame: Within 6 months from the enrollment

Number of spontaneous pregnancies conceived per women diagnosed by transvaginal ultrasound. Diagnosis is based on the identification of intrauterine gestational sac with embryo and/or yolk sac.

Spontaneous ovulation rate

Time Frame: Change in spontaneous ovulation rate, through study completion (an average of 18 months)

Spontaneous ovulation activity evaluated by menstrual cycle regularization. Menstrual cycles evaluated by intervals between menstruations (days), day of menstrual blood flow. Rate evaluate considering the number of women with restored regular menstrual cycles per women with irregular menstrual cycles.

Secondary Outcomes

  • Glucose metabolism(Change in glucose metabolism, through study completion (an average of 18 months))
  • BMI(Change in BMI, through study completion (an average of 18 months))
  • Lipid metabolism(Change in Lipid metabolism, through study completion (an average of 18 months))
  • Androgens profile(Change in Androgens profile, through study completion (an average of 18 months))
  • Blood pressure(Change in Blood pressure, through study completion (an average of 18 months))

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