Skip to content

D-chiroinositol Administration in Hypogonadal Males

D-chiroinositol Administration for Testosterone Level Improvement in Hypogonadal Males

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04708249
Enrollment
10
Registered
2021-01-13
Start date
2021-01-18
Completion date
2021-03-01
Last updated
2021-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Male Hypogonadism, Sexual Dysfunction

Keywords

Male Hypogonadism, Testosterone, Aromatase, D-chiroinositol, Sexual dysfunction

Brief summary

D-chiroinositol (DCI), is known as second messenger of insulin pathway, but recently several works have reported the influence of DCI on steroidogenesis. In particular, the DCI capabilities to regulate aromatase expression and testosterone biosynthesis are arising. In this regard, DCI administration in case of reduced levels of testosterone, could be a good therapeutic opportunity. For this reason, the treatment of Late-Onset Male Hypogonadism (LOH) in undoubtedly an interesting target. LOH is a reduction of testosterone level due to advancing age, currently treated with Testosterone Replacement Therapy (TRT). Unfortunately, there is a lack of information about TRT safety, especially in older men. For these reasons, the aim of this study is to evaluate the effect of DCI treatment on testosterone accumulation in LOH patient.

Interventions

DIETARY_SUPPLEMENTD-chiroinositol

Supplementation with 600 mg of D-chiroinositol, two-times daily on an empty stomach, for 30 days.

Sponsors

Lo.Li.Pharma s.r.l
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
65 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Men, with a diagnosis of Late-Onset Male Hypogonadism * Insulin resistance (HOMA Index \> 2,5) * BMI between 25 and 30

Exclusion criteria

* Alcohol intake and/or drug abuse * Recent hormonal treatment * Smoking * Obesity * Systemic or endocrine diseases * Male accessory gland infection * Clinical history of cryptorchidism or varicocele and micro-orchidism

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Serum Testosterone at 1 monthAt baseline and after 30 days of treatmentLevel of testosterone detected in the blood in ng/dL

Secondary

MeasureTime frameDescription
Change from Baseline Weight at 1 monthAt baseline and after 30 days of treatmentBody weight of patients reported in kg
Change from Baseline BMI at 1 monthAt baseline and after 30 days of treatmentBody Mass Index of patients calculated as kg/m2, where kg is the weight measured for eah patient while m2 is his height squared
Change from Baseline Insulin at 1 monthAt baseline and after 30 days of treatmentLevel of fasting insulin detected in the blood and reported in microU/L
Change from Baseline Glycaemia at 1 monthAt baseline and after 30 days of treatmentLevel of fasting glycaemia detected in the blood and reported in mg/dL
Change from Baseline HOMA index at 1 monthAt baseline and after 30 days of treatmentHOMA index known as Homeostatic Model Assessment for Insulin Resistance is: (fasting glycaemia x fasting insulin)/405
Change from Baseline Waist circumference at 1 monthAt baseline and after 30 days of treatmentWaist circumference of patients reported in cm
Change from Baseline Luteinizing Hormone at 1 monthAt baseline and after 30 days of treatmentLevel of luteinizing hormone detected in the blood and reported in mUI/ml
Change from Baseline Oestradiol at 1 monthAt baseline and after 30 days of treatmentLevel of oestradiol detected in the blood and reported in pg/mL
Change from Baseline Oestrone at 1 monthAt baseline and after 30 days of treatmentLevel of oestrone detected in the blood and reported in pg/mL
Change from Baseline Testosterone/Oestradiol ratio at 1 monthAt baseline and after 30 days of treatmentRatio between the levels of oestradiol and testosterone detected in the blood
Change from Baseline Strength Test at 1 monthAt baseline and after 30 days of treatmentMeasurement of strength performed with the dominant hand using a hand-held dynamometer (Good Strength, IGS01, Metitur Oy, Jyväskylä, Finland) with the participant in the seated position with elbow flexed at 110°. The participant will be instructed to squeeze the handle as hard as possible for 3-5 seconds and the stregth will be recorded in kg
Change from Baseline Androstenedione at 1 monthAt baseline and after 30 days of treatmentLevel of androstenedione detected in the blood and reported in ng/mL

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026