ClinicalTrials.Veeva

Menu

Myo-inositol, Alpha-Lactalbumin and Folic Acid Treatment in PCOS

A

AGUNCO Obstetrics and Gynecology Centre

Status

Completed

Conditions

Polycystic Ovary Syndrome

Treatments

Dietary Supplement: myo-inositol, alpha-lactalbumin, folic acid

Study type

Interventional

Funder types

Other

Identifiers

NCT04645745
UVittorio

Details and patient eligibility

About

The main aim of this study is to evaluate the effect of myo-inositol and alpha-lactalbumin treatment on HOMA-index improvement in two different groups of women, belonging to the Mexican and Italian population, both affected by Polycystic Ovary Syndrome.

Full description

This is an open-label clinical trial aimed at evaluating and comparing the effect of myo-inositol and alpha-lactalbumin treatment on HOMA-index improvement in two different groups of PCOS patients from the Mexican and Italian population. The addition of alpha-lactalbumin helps to increase the intestinal absorption of myo-inositol and consequently improve its effect. The scientific evidence so far available shows that these two groups of PCOS women have a different genetic, nutritional, and behavioural profile. Important factors are body mass index and insulin resistance, both increased in the Mexican women, although among them PCOS prevalence is not higher compared to many other populations. Therefore, the focus of this study is to check the effects of the combined administration of myo-inositol and alpha-lactalbumin for six months (with a control at three months) e to compare these effects between the two groups of patients, monitoring several hormonal parameters connected to the menstrual cycle regularization.

Enrollment

36 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • PCOS diagnosis based on the Rotterdam ESHRE-ASRM consensus workshop group1.
  • Presence of Insulin resistance diagnosed by HOMA-Index
  • Patients belonging to the Mexican population
  • Patients belonging to the Italian population

Exclusion criteria

  • BMI ≥ 30
  • Other conditions causing ovulatory disorders and/or androgens hyper production such as: hyperprolactinemia, hypothyroidism, adrenal hyperplasia and Cushing syndrome
  • Hormonal and/or pharmacological treatments in the previous 3 months that could interfere with ovulation
  • Drastic changes in diet and physical activity
  • Treatment with products containing inositols in the previous 3 months

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

36 participants in 1 patient group

myo-inositol plus alpha-lactalbumin
Experimental group
Description:
Patients were treated with 2 g myo-inositol, 50 mg alpha-LA and 200 mcg of Folic Acid twice a day for 6 months. Controls were the same patients at baseline (t0)
Treatment:
Dietary Supplement: myo-inositol, alpha-lactalbumin, folic acid

Trial contacts and locations

2

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems