Skip to main content
Clinical Trials/NCT01246310
NCT01246310
Terminated
Not Applicable

Myoinositol for the Treatment of Ovarian and Psychiatric Disorder in PCOS Patients.

AGUNCO Obstetrics and Gynecology Centre1 site in 1 country24 target enrollmentNovember 2010
ConditionsDepressionPCOS

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depression
Sponsor
AGUNCO Obstetrics and Gynecology Centre
Enrollment
24
Locations
1
Primary Endpoint
Short form of Mc Gill Pain Questionnaire
Status
Terminated
Last Updated
4 years ago

Overview

Brief Summary

Polycystic ovary syndrome (PCOS) is one of the most common reproductive disorders affecting 5-10% of women of reproductive age. Beside impairments on reproductive functions (oligomenorrhea/amenorrhea), it also affects metabolism (insulin resistance, type 2 diabetes mellitus and cardiovascular risk) and psychology (increased anxiety, depression and eating disorders). Recently, several studies have shown that there is an increased risk of mood disorders in women with PCOS, with major depression and bipolar disorder as the most frequent diagnosis.

Myo-inositol is classified as a member of the vitamin B complex and it works as a second messenger system of several neurotransmitter receptors; furthermore, inositol, when administrated at pharmacological doses, crosses the blood-brain barrier.

Studies from the 90s showed that inositol, alone or in combination with other antidepressant drugs (mainly serotonin reuptake inhibitors), is able to induce improvement of the Hamilton depression rating Scale.

Recently, inositol has been proposed as treatment to improve clinical, metabolic and endocrinal status in PCOS patients. Administration of myo-inositol to PCOs patients resulted in several beneficial effects, such as decrease of circulating insulin and serum total testosterone as well as a restored ovulation.

In this proposed study, the investigators aim to evaluate in a double blind randomized trial whether inositol alone has beneficial effects on mental health disorders associated with PCOs. In particular, 60 women in reproductive age that will be diagnosed of PCOs, according to Rotterdam 2003 criteria, will be recruited and randomly assigned to the inositol or placebo group. Both groups will go through ultrasonic evaluation of the ovaries and serum hormonal levels (FSH, LH, testosterone, estradiol and insulin) will be evaluated. Furthermore, with the help of psychiatrics, patients will be interviewed in order to test the presence of any mental health disorders using validated tests such as: Hamilton Anxiety Scale (HAM-A), Hamilton Rating Scale for Depression (HAM-D), Health Assessment Questionnaire (HAQ), Short Form of Mc Gill Pain Questionnaire (SF-MPQ).

Women assigned to the inositol group will receive 12g of inositol during the day in three different administrations for a period of 4weeks.

At the end of treatment period patients will be interviewed by psychiatrics and will go through ultrasonic evaluation of the ovaries and hormonal levels will be tested

Registry
clinicaltrials.gov
Start Date
November 2010
End Date
February 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
AGUNCO Obstetrics and Gynecology Centre
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Women diagnosed of PCOS according to Rotterdam 2003 criteria

Exclusion Criteria

  • Pharmacological treatment in the last 3 moths
  • Use of contraceptive pill

Outcomes

Primary Outcomes

Short form of Mc Gill Pain Questionnaire

Hamilton Anxiety Scale

Health assessment Questionnaire

Hamilton Rating Scale for depression

Study Sites (1)

Loading locations...

Similar Trials