Myoinositol Plus L-tyrosine, Selenium and Chromium in PCOS

NCT ID: NCT03673995

Last Updated: 2020-06-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

186 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-05-02

Study Completion Date

2018-10-30

Brief Summary

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PCOS patients were treated every day, with one sachet containing 2000 mg myo-inositol, 500 mg L-tyrosine, 40 mcg chromium picolinate, 55 mcg selenium, 200 mcg folic acid. All patients underwent, before starting the therapy, after 3 months and 6 months, hormonal evaluation , hirsutism scoring and ovulation assesment. Most of them during the treatment improved their symptoms.

Detailed Description

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Conditions

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Polycystic Ovary Syndrome Menstrual Problem Hirsutism

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Myo-inositol+L-tyrosine

One sachet per day containing 2000 mg myo-inositol, 500 mg L-tyrosine, 40 mcg chromium picolinate, 55 mcg selenium, 200 mcg folic acid for improving PCOS symptoms.

Group Type EXPERIMENTAL

Myo-inositol+L-tyrosine

Intervention Type DIETARY_SUPPLEMENT

PCOS patients were treated every day, with one sachet containing 2000 mg myo-inositol, 500 mg L-tyrosine, 40 mcg chromium picolinate, 55 mcg selenium, 200 mcg folic acid. All patients underwent, before starting the therapy, after 3 months and 6 months, hormonal, hirsutism and ovulation assesment.

Interventions

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Myo-inositol+L-tyrosine

PCOS patients were treated every day, with one sachet containing 2000 mg myo-inositol, 500 mg L-tyrosine, 40 mcg chromium picolinate, 55 mcg selenium, 200 mcg folic acid. All patients underwent, before starting the therapy, after 3 months and 6 months, hormonal, hirsutism and ovulation assesment.

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

° PCOS patients

Exclusion Criteria

* thyroid dysfunction
* hyperprolactinemia
* adrenal hyperplasia
* patients taking oral contraceptive
* any other endocrinological pathologies
Minimum Eligible Age

16 Years

Maximum Eligible Age

38 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Pharmarte srl

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Mario Montanino Oliva, M.D.

Role: PRINCIPAL_INVESTIGATOR

Altamedica Reproductive Medicine

Locations

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Altamedica Reproductive Medicine

Roma, , Italy

Site Status

Countries

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Italy

Other Identifiers

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PharmarteLtyrosine1

Identifier Type: -

Identifier Source: org_study_id

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