D-chiro-inositol and Endometrial Thickness

N/ACompletedNCT05283642

Lo.Li.Pharma s.r.l13 enrolled

Overview

Investigation of the effects of D-chiro-inositol supplementation in women with altered endometrial thickness.

Study Type

INTERVENTIONAL

Allocation

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

Endometrial Diseases

Interventions

DCIDIETARY_SUPPLEMENT

Oral supplementation with D-chiro-inositol once daily

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 60 Years

Medical Language ↔ Plain English

Inclusion Criteria: \- altered endometrial thickness Exclusion Criteria: * patients with cancer * patients under hormonal treatments (progestogens and/or estrogens) * patients supplemented with inositols

Locations (1)

ASL Umbria 2

Terni, Umbria, Italy

Outcomes

Primary Outcomes

Change in endometrial thickness

Change in endometrial thickness by ultrasound measurement from baseline to three months

Time frame: Two time points: baseline and after three months

Data from ClinicalTrials.gov

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