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Clinical Trial Summary

Ovarian hyperstimulation syndrome (OHSS), although quite uncommon, represents the most serious complication of ovulation induction during in-vitro fertilization (IVF) protocols. The syndrome is triggered by exaggerated ovarian response to gonadotropins, which eventually leads to pathological manifestations that range from mild symptoms, such as abdominal discomfort, to life-threatening complications in the most severe cases. Prevention is paramount during fertilization programs and requires assessment of risk factors and close monitoring of risk markers. Clinicians quite generally consider unusually elevated estrogen levels as both indicator for OHSS and one possible etiological factor. In this scenario, myo-inositol (MYO) treatment proved to reduce the amount of FSH units and the duration of the stimulation protocol, decreasing the risk of OHSS onset. On the other hand, inconclusive evidence is available about the effect of D-chiro-inositol (DCI) supplementation within assisted reproductive treatments. The aim of the proposed pilot study is to assess the effect of DCI supplementation on the doses of FSH used in IVF-ET protocols, also with respect to MYO treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Amount of FSH Units During Ovarian Stimulation Protocols

NCT number NCT04576546
Study type Interventional
Source Lo.Li.Pharma s.r.l
Contact Cesare Aragona, MD
Phone +39 348 4043527
Email aragonacesare@gmail.com
Status Recruiting
Phase N/A
Start date November 2, 2020
Completion date June 2022